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C07D 413/12 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links 14
C07D 413/14 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings 11
C07D 239/48 - Two nitrogen atoms 10
C07D 403/12 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a chain containing hetero atoms as chain links 10
A61K 31/505 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim 8
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Found results for  patents

1.

DIAMINOPYRIMIDINES AS P2X3 AND P2X2/3 ANTAGONISTS

      
Application Number 18890411
Status Pending
Filing Date 2024-09-19
First Publication Date 2025-02-27
Owner Roche Palo Alto LLC (USA)
Inventor
  • Broka, Chris Allen
  • Carter, David Scott
  • Dillon, Michael Patrick
  • Hawley, Ronald Charles
  • Jahangir, Alam
  • Lin, Clara Jeou Jen
  • Parish, Daniel Warren

Abstract

Compounds and methods for treating diseases mediated by a P2X3 and/or a P2X2/3 receptor antagonist, the methods comprising administering to a subject in need thereof an effective amount of a compound of formula (I): Compounds and methods for treating diseases mediated by a P2X3 and/or a P2X2/3 receptor antagonist, the methods comprising administering to a subject in need thereof an effective amount of a compound of formula (I): Compounds and methods for treating diseases mediated by a P2X3 and/or a P2X2/3 receptor antagonist, the methods comprising administering to a subject in need thereof an effective amount of a compound of formula (I): or a pharmaceutically acceptable salt, solvate or prodrug thereof, wherein X is O, D, Y, R1, R2, R3, R4, R5, R6, R7 and R8 are as defined herein.

IPC Classes  ?

  • C07D 239/49 - Two nitrogen atoms with an aralkyl radical, or substituted aralkyl radical, attached in position 5, e.g. trimethoprim
  • A61K 31/505 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim
  • A61K 31/506 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
  • C07D 239/48 - Two nitrogen atoms
  • C07D 403/12 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 405/12 - Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 409/12 - Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 413/12 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 417/12 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a chain containing hetero atoms as chain links

2.

METHODS OF USING DIAMINOPYRIMIDINE P2X3 AND P2X2/3 RECEPTOR MODULATORS FOR TREATMENT OF RESPIRATORY AND GASTROINTESTINAL DISEASES

      
Application Number 18779395
Status Pending
Filing Date 2024-07-22
First Publication Date 2025-01-23
Owner Roche Palo Alto LLC (USA)
Inventor
  • Broka, Chris Allen
  • Carter, David Scott
  • Dillon, Michael Patrick
  • Ford, Anthony P.D.W.
  • Hawley, Ronald Charles
  • Jahangir, Alam
  • Moore, Amy Geraldine
  • Parish, Daniel Warren

Abstract

Methods for treating respiratory and gastrointestinal diseases mediated by a P2X3 and/or a P2X2/3 receptor antagonist, the methods comprising administering to a subject in need thereof an effective amount of a compound of formula (I): Methods for treating respiratory and gastrointestinal diseases mediated by a P2X3 and/or a P2X2/3 receptor antagonist, the methods comprising administering to a subject in need thereof an effective amount of a compound of formula (I): Methods for treating respiratory and gastrointestinal diseases mediated by a P2X3 and/or a P2X2/3 receptor antagonist, the methods comprising administering to a subject in need thereof an effective amount of a compound of formula (I): or a pharmaceutically acceptable salt thereof, wherein D, X, Y, R1, R2, R3, R4, R5, R6, R7 and R8 are as defined herein.

IPC Classes  ?

  • A61K 31/506 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
  • A61K 31/505 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim
  • A61K 31/513 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim having oxo groups directly attached to the heterocyclic ring, e.g. cytosine
  • A61K 31/538 - 1,4-Oxazines, e.g. morpholine ortho- or peri-condensed with carbocyclic ring systems

3.

DIAMINOPYRIMIDINES AS P2X3 AND P2X2/3 ANTAGONISTS

      
Application Number 18308282
Status Pending
Filing Date 2023-04-27
First Publication Date 2024-05-16
Owner Roche Palo Alto LLC (USA)
Inventor
  • Broka, Chris Allen
  • Carter, David Scott
  • Dillon, Michael Patrick
  • Hawley, Ronald Charles
  • Jahangir, Alam
  • Lin, Clara Jeou Jen
  • Parish, Daniel Warren

Abstract

Compounds and methods for treating diseases mediated by a P2X3 and/or a P2X2/3 receptor antagonist, the methods comprising administering to a subject in need thereof an effective amount of a compound of formula (I): Compounds and methods for treating diseases mediated by a P2X3 and/or a P2X2/3 receptor antagonist, the methods comprising administering to a subject in need thereof an effective amount of a compound of formula (I): Compounds and methods for treating diseases mediated by a P2X3 and/or a P2X2/3 receptor antagonist, the methods comprising administering to a subject in need thereof an effective amount of a compound of formula (I): or a pharmaceutically acceptable salt, solvate or prodrug thereof, wherein X is O, D, Y, R1, R2, R3, R4, R5, R6, R7 and R8 are as defined herein.

IPC Classes  ?

  • C07D 239/49 - Two nitrogen atoms with an aralkyl radical, or substituted aralkyl radical, attached in position 5, e.g. trimethoprim
  • A61K 31/505 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim
  • C07D 239/48 - Two nitrogen atoms
  • C07D 403/12 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 405/12 - Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 409/12 - Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 413/12 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 417/12 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a chain containing hetero atoms as chain links

4.

Method for improving pharmacokinetics

      
Application Number 16842855
Grant Number 10918626
Status In Force
Filing Date 2020-04-08
First Publication Date 2020-07-23
Grant Date 2021-02-16
Owner Roche Palo Alto LLC (USA)
Inventor Tran, Jonathan Q.

Abstract

The object of the present invention is to inhibit oxidative metabolism of a compound of formula I by co-administration with ritonavir, a cytochrome P450 inhibitor.

IPC Classes  ?

  • A61K 31/426 - 1,3-Thiazoles
  • A61K 31/404 - Indoles, e.g. pindolol
  • A61K 45/06 - Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
  • A61K 31/407 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with heterocyclic ring systems, e.g. ketorolac, physostigmine

5.

2/3 antagonists

      
Application Number 15459361
Grant Number 09849136
Status In Force
Filing Date 2017-03-15
First Publication Date 2017-06-29
Grant Date 2017-12-26
Owner Roche Palo Alto LLC (USA)
Inventor
  • Chen, Li
  • Dillon, Michael Patrick
  • Feng, Lichun
  • Hawley, Ronald Charles
  • Yang, Minmin

Abstract

2/3 receptor with compounds of the formula I: b are as defined herein.

IPC Classes  ?

  • A01N 61/00 - Biocides, pest repellants or attractants, or plant growth regulators containing substances of unknown or undetermined composition, e.g. substances characterised only by the mode of action
  • A61K 31/00 - Medicinal preparations containing organic active ingredients
  • A61K 31/5377 - 1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
  • A61K 31/426 - 1,3-Thiazoles
  • A61K 31/428 - Thiazoles condensed with carbocyclic rings
  • A61K 31/421 - 1,3-Oxazoles, e.g. pemoline, trimethadione
  • A61K 31/42 - Oxazoles
  • A61K 31/425 - Thiazoles
  • A61K 31/501 - PyridazinesHydrogenated pyridazines not condensed and containing further heterocyclic rings

6.

2/3 antagonists

      
Application Number 15422121
Grant Number 10201525
Status In Force
Filing Date 2017-02-01
First Publication Date 2017-05-25
Grant Date 2019-02-12
Owner Roche Palo Alto LLC (USA)
Inventor
  • Dillon, Michael Patrick
  • Hawley, Ronald Charles
  • Chen, Li
  • Feng, Lichun
  • Yang, Minmin

Abstract

2/3 receptors treating a patient with a compound of formula I 2/3 receptor antagonist and methods of making the compounds.

IPC Classes  ?

  • A61K 31/41 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which is nitrogen, e.g. tetrazole
  • A61K 31/4439 - Non-condensed pyridinesHydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
  • A61K 31/497 - Non-condensed pyrazines containing further heterocyclic rings
  • A61K 31/5377 - 1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
  • C07D 257/04 - Five-membered rings
  • C07D 401/10 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing aromatic rings
  • C07D 403/10 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a carbon chain containing aromatic rings
  • C07D 403/14 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group containing three or more hetero rings
  • C07D 405/12 - Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 407/10 - Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a carbon chain containing aromatic rings
  • C07D 413/10 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
  • C07D 417/10 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a carbon chain containing aromatic rings
  • C07D 491/10 - Spiro-condensed systems
  • C07D 241/12 - Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
  • C07D 401/12 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 401/14 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
  • C07D 403/12 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 409/12 - Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 417/12 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 471/04 - Ortho-condensed systems
  • C07D 491/107 - Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
  • C07D 498/08 - Bridged systems

7.

Thiazole and oxazole-substituted arylamides as P2X3 and P2X2/3 antagonists

      
Application Number 15093320
Grant Number 09617254
Status In Force
Filing Date 2016-04-07
First Publication Date 2016-08-04
Grant Date 2017-04-11
Owner Roche Palo Alto LLC (USA)
Inventor
  • Chen, Li
  • Dillon, Michael Patrick
  • Feng, Lichun
  • Hawley, Ronald Charles
  • Yang, Minmin

Abstract

Compounds of the formula I: 1 is a group of formula A or formula B, 2/3 receptor antagonist and methods of making the subject compounds.

IPC Classes  ?

  • A01N 61/00 - Biocides, pest repellants or attractants, or plant growth regulators containing substances of unknown or undetermined composition, e.g. substances characterised only by the mode of action
  • A61K 31/00 - Medicinal preparations containing organic active ingredients
  • C07D 417/14 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group containing three or more hetero rings
  • C07D 261/08 - Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
  • C07D 263/32 - Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
  • C07D 275/02 - Heterocyclic compounds containing 1, 2-thiazole or hydrogenated 1,2-thiazole rings not condensed with other rings
  • C07D 277/30 - Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
  • C07D 277/66 - Benzothiazoles with only hydrocarbon or substituted hydrocarbon radicals attached in position 2 with aromatic rings or ring systems directly attached in position 2
  • C07D 417/12 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 277/56 - Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
  • C07D 413/14 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
  • C07D 417/10 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a carbon chain containing aromatic rings

8.

Tetralin and indane derivatives and uses thereof

      
Application Number 14531465
Grant Number 09670151
Status In Force
Filing Date 2014-11-03
First Publication Date 2015-09-24
Grant Date 2017-06-06
Owner Roche Palo Alto LLC (USA)
Inventor
  • Greenhouse, Robert
  • Harris, Iii, Ralph New
  • Jaime-Figueroa, Saul
  • Kress, James M.
  • Repke, David Bruce
  • Stabler, Russell Stephen

Abstract

Compounds of the formula I: 2 are as defined herein. Also provided are methods for preparing, compositions comprising, and methods for using compounds of formula I.

IPC Classes  ?

  • C07C 317/32 - SulfonesSulfoxides having sulfone or sulfoxide groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton with sulfone or sulfoxide groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
  • C07C 317/44 - SulfonesSulfoxides having sulfone or sulfoxide groups and carboxyl groups bound to the same carbon skeleton
  • C07D 207/16 - Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
  • C07D 207/325 - Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms with substituted hydrocarbon radicals directly attached to the ring nitrogen atom
  • C07D 207/34 - Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
  • C07D 207/36 - Oxygen or sulfur atoms
  • C07D 209/30 - IndolesHydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
  • C07D 231/18 - One oxygen or sulfur atom
  • C07D 233/20 - Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with substituted hydrocarbon radicals, directly attached to ring carbon atoms
  • C07D 233/34 - Ethylene-urea
  • C07D 233/48 - Nitrogen atoms not forming part of a nitro radical with acyclic hydrocarbon or substituted acyclic hydrocarbon radicals, attached to said nitrogen atoms
  • C07D 233/54 - Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
  • C07D 233/64 - Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
  • C07D 233/84 - Sulfur atoms
  • C07D 233/88 - Nitrogen atoms, e.g. allantoin
  • C07D 233/90 - Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
  • C07D 235/06 - BenzimidazolesHydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
  • C07D 239/14 - Nitrogen atoms not forming part of a nitro radical with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, attached to said nitrogen atoms
  • C07D 239/42 - One nitrogen atom
  • C07D 277/82 - Nitrogen atoms
  • C07D 233/44 - Nitrogen atoms not forming part of a nitro radical
  • C07D 233/58 - Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring nitrogen atoms

9.

2/3 antagonists

      
Application Number 14547632
Grant Number 09505726
Status In Force
Filing Date 2014-11-19
First Publication Date 2015-03-19
Grant Date 2016-11-29
Owner Roche Palo Alto LLC (USA)
Inventor
  • Broka, Chris Allen
  • Hawley, Ronald Charles

Abstract

Compounds of the formula I: 2/3 receptor antagonists and methods of making the compounds.

IPC Classes  ?

  • A61K 31/166 - Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the carbon atom of a carboxamide group directly attached to the aromatic ring, e.g. procainamide, procarbazine, metoclopramide, labetalol
  • C07C 233/64 - Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings
  • C07D 241/12 - Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
  • C07C 237/32 - Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton having the nitrogen atom of the carboxamide group bound to an acyclic carbon atom of a hydrocarbon radical substituted by oxygen atoms
  • C07D 265/30 - 1,4-OxazinesHydrogenated 1,4-oxazines not condensed with other rings
  • C07D 405/14 - Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
  • C07D 417/12 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07C 237/42 - Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton having nitrogen atoms of amino groups bound to the carbon skeleton of the acid part, further acylated
  • C07D 213/56 - Amides
  • C07D 213/61 - Halogen atoms or nitro radicals
  • C07D 213/81 - AmidesImides
  • C07D 231/14 - Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
  • C07D 241/24 - Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
  • C07D 261/18 - Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen
  • C07D 263/34 - Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
  • C07D 277/56 - Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
  • C07D 285/06 - 1,2,3-ThiadiazolesHydrogenated 1,2,3-thiadiazoles
  • C07D 295/125 - Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
  • C07D 307/68 - Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
  • C07D 309/08 - Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
  • C07D 333/38 - Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
  • C07D 401/12 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 403/12 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a chain containing hetero atoms as chain links

10.

2/3 antagonists

      
Application Number 14459143
Grant Number 09512089
Status In Force
Filing Date 2014-08-13
First Publication Date 2015-03-05
Grant Date 2016-12-06
Owner Roche Palo Alto LLC (USA)
Inventor
  • Chen, Li
  • Dillon, Michael Patrick
  • Feng, Lichun
  • Hawley, Ronald Charles
  • Yang, Minmin

Abstract

Compounds of the formula I: 2/3 receptor antagonist and methods of making the compounds.

IPC Classes  ?

  • A01N 43/64 - Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
  • A61K 31/41 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which is nitrogen, e.g. tetrazole
  • C07D 401/00 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
  • C07D 403/00 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group
  • C07D 405/00 - Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
  • C07D 409/00 - Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
  • C07D 257/04 - Five-membered rings
  • C07D 401/10 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing aromatic rings
  • C07D 401/14 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
  • C07D 405/12 - Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 409/14 - Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
  • C07D 471/04 - Ortho-condensed systems
  • C07D 413/12 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links

11.

2/3 antagonists

      
Application Number 14328959
Grant Number 09512112
Status In Force
Filing Date 2014-07-11
First Publication Date 2014-10-30
Grant Date 2016-12-06
Owner Roche Palo Alto LLC (USA)
Inventor
  • Chen, Li
  • Dillon, Michael Patrick
  • Feng, Lichun
  • Yang, Minmin

Abstract

Compounds of the formula I: 2/3 receptor antagonists and methods of making the compounds.

IPC Classes  ?

  • C07D 401/02 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
  • C07D 413/12 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 207/27 - 2-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms with substituted hydrocarbon radicals directly attached to the ring nitrogen atom
  • C07D 233/32 - One oxygen atom
  • C07D 263/20 - Oxygen atoms attached in position 2
  • C07D 407/14 - Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group containing three or more hetero rings
  • C07D 413/10 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
  • C07D 413/14 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
  • C07D 473/00 - Heterocyclic compounds containing purine ring systems
  • C07D 403/12 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a chain containing hetero atoms as chain links

12.

Process for synthesis of phenoxy diaminopyrimidine derivatives

      
Application Number 14053362
Grant Number 09643934
Status In Force
Filing Date 2013-10-14
First Publication Date 2014-02-13
Grant Date 2017-05-09
Owner Roche Palo Alto LLC (USA)
Inventor
  • Dvorak, Charles Alois
  • Green, Keena Lynn
  • Lee, Gary R.

Abstract

A method for preparing a compound of formula k the method comprising treating a compound of formula j with ammonia, to form the compound of formula k.

IPC Classes  ?

13.

Isoxazolo-pyridine derivatives

      
Application Number 13916264
Grant Number 08877783
Status In Force
Filing Date 2013-06-12
First Publication Date 2013-10-24
Grant Date 2014-11-04
Owner Roche Palo Alto LLC (USA)
Inventor
  • Buettelmann, Bernd
  • Jakob-Roetne, Roland
  • Knust, Henner
  • Lucas, Matthew C.
  • Thomas, Andrew

Abstract

The present invention is concerned with isoxazole-pyridine derivatives of formula I 6 are as described herein. The compounds are active on the GABA A α5 receptor binding site and useful for the treatment of cognitive disorders, such as Alzheimer's disease.

IPC Classes  ?

  • A61K 31/4427 - Non-condensed pyridinesHydrogenated derivatives thereof containing further heterocyclic ring systems
  • C07D 413/12 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 487/04 - Ortho-condensed systems
  • C07D 417/14 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group containing three or more hetero rings
  • C07D 491/10 - Spiro-condensed systems
  • C07D 413/14 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
  • C07D 491/08 - Bridged systems

14.

Isoxazolo-pyridine derivatives

      
Application Number 13916068
Grant Number 08846719
Status In Force
Filing Date 2013-06-12
First Publication Date 2013-10-17
Grant Date 2014-09-30
Owner Roche Palo Alto LLC (USA)
Inventor
  • Buettelmann, Bernd
  • Jakob-Roetne, Roland
  • Knust, Henner
  • Lucas, Matthew C.
  • Thomas, Andrew

Abstract

The present invention is concerned with isoxazole-pyridine derivatives of formula I 6 are as described herein. The compounds are active on the GABA A α5 receptor binding site and useful for the treatment of cognitive disorders, such as Alzheimer's disease.

IPC Classes  ?

  • A61K 31/4427 - Non-condensed pyridinesHydrogenated derivatives thereof containing further heterocyclic ring systems
  • C07D 413/12 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links

15.

Isoxazolo-pyridine derivatives

      
Application Number 13916191
Grant Number 08877782
Status In Force
Filing Date 2013-06-12
First Publication Date 2013-10-17
Grant Date 2014-11-04
Owner Roche Palo Alto LLC (USA)
Inventor
  • Buettelmann, Bernd
  • Jakob-Roetne, Roland
  • Knust, Henner
  • Lucas, Matthew C.
  • Thomas, Andrew

Abstract

The present invention is concerned with isoxazole-pyridine derivatives of formula I 6 are as described herein. The compounds are active on the GABA A α5 receptor binding site and useful for the treatment of cognitive disorders, such as Alzheimer's disease.

IPC Classes  ?

  • A61K 31/4427 - Non-condensed pyridinesHydrogenated derivatives thereof containing further heterocyclic ring systems
  • C07D 413/12 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 491/10 - Spiro-condensed systems
  • C07D 413/14 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
  • C07D 487/04 - Ortho-condensed systems
  • C07D 491/08 - Bridged systems
  • C07D 417/14 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group containing three or more hetero rings

16.

Isoxazolo-pyridine derivatives

      
Application Number 13916317
Grant Number 09073908
Status In Force
Filing Date 2013-06-12
First Publication Date 2013-10-17
Grant Date 2015-07-07
Owner ROCHE PALO ALTO LLC (USA)
Inventor
  • Buettelmann, Bernd
  • Jakob-Roetne, Roland
  • Knust, Henner
  • Lucas, Matthew C.
  • Thomas, Andrew

Abstract

The present invention is concerned with isoxazole-pyridine derivatives of formula I 6 are as described herein. The compounds are active on the GABA A α5 receptor binding site and useful for the treatment of cognitive disorders, such as Alzheimer's disease.

IPC Classes  ?

  • A61K 31/422 - Oxazoles not condensed and containing further heterocyclic rings
  • C07D 261/08 - Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
  • C07D 413/12 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 413/14 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
  • C07D 417/14 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group containing three or more hetero rings
  • C07D 487/04 - Ortho-condensed systems
  • C07D 491/08 - Bridged systems
  • C07D 491/10 - Spiro-condensed systems

17.

2/3 antagonists

      
Application Number 13911369
Grant Number 09440956
Status In Force
Filing Date 2013-06-06
First Publication Date 2013-10-10
Grant Date 2016-09-13
Owner Roche Palo Alto LLC (USA)
Inventor
  • Dillon, Michael Patrick
  • Krauss, Nancy Elisabeth

Abstract

Compounds of the formula I: 2/3 receptor antagonists and methods of making the compounds.

IPC Classes  ?

  • C07D 401/04 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring- member bond
  • C07D 401/14 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
  • C07D 209/08 - IndolesHydrogenated indoles with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to carbon atoms of the hetero ring
  • C07D 401/10 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing aromatic rings

18.

Pyridinyl amides as P2X3 and P2X2/3 inhibitors

      
Application Number 13592625
Grant Number 08895589
Status In Force
Filing Date 2012-08-23
First Publication Date 2013-06-27
Grant Date 2014-11-25
Owner Roche Palo Alto LLC (USA)
Inventor
  • Broka, Chris Allen
  • Hawley, Ronald Charles

Abstract

Compounds of the formula I: 2/3 receptor antagonists and methods of making the compounds.

IPC Classes  ?

  • A61K 31/4418 - Non-condensed pyridinesHydrogenated derivatives thereof having a carbocyclic ring directly attached to the heterocyclic ring, e.g. cyproheptadine
  • C07D 213/24 - Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
  • C07D 405/14 - Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
  • C07D 417/12 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 307/68 - Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
  • C07D 265/30 - 1,4-OxazinesHydrogenated 1,4-oxazines not condensed with other rings
  • C07D 403/12 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 261/18 - Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen
  • C07D 213/56 - Amides
  • C07D 263/34 - Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
  • C07D 213/61 - Halogen atoms or nitro radicals
  • C07D 277/56 - Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
  • C07C 237/42 - Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton having nitrogen atoms of amino groups bound to the carbon skeleton of the acid part, further acylated
  • C07D 333/38 - Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
  • C07D 213/81 - AmidesImides
  • C07D 241/24 - Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
  • C07C 237/32 - Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton having the nitrogen atom of the carboxamide group bound to an acyclic carbon atom of a hydrocarbon radical substituted by oxygen atoms
  • C07D 241/12 - Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
  • C07D 309/08 - Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
  • C07D 231/14 - Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
  • C07D 285/06 - 1,2,3-ThiadiazolesHydrogenated 1,2,3-thiadiazoles
  • C07D 295/125 - Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
  • C07D 401/12 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links

19.

Isoxazolo-pyridine derivatives

      
Application Number 13370444
Grant Number 08518974
Status In Force
Filing Date 2012-02-10
First Publication Date 2012-07-19
Grant Date 2013-08-27
Owner ROCHE PALO ALTO LLC (USA)
Inventor
  • Buettelmann, Bernd
  • Jakob-Roetne, Roland
  • Knust, Henner
  • Lucas, Matthew C.
  • Thomas, Andrew

Abstract

The present invention is concerned with isoxazole-pyridine derivatives of formula I 6 are as described herein. The compounds are active on the GABA A α5 receptor binding site and useful for the treatment of cognitive disorders, such as Alzheimer's disease.

IPC Classes  ?

  • A61K 31/4427 - Non-condensed pyridinesHydrogenated derivatives thereof containing further heterocyclic ring systems
  • C07D 413/12 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links

20.

2/3 antagonists

      
Application Number 13359330
Grant Number 09173861
Status In Force
Filing Date 2012-01-26
First Publication Date 2012-05-17
Grant Date 2015-11-03
Owner Roche Palo Alto LLC (USA)
Inventor
  • Chen, Li
  • Feng, Lichun
  • Yang, Minmin
  • Dillon, Michael Patrick
  • Lai, Yingjie

Abstract

Compounds of the formula I: 2/3 receptor antagonists and methods of making the compounds.

IPC Classes  ?

  • A61K 31/166 - Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the carbon atom of a carboxamide group directly attached to the aromatic ring, e.g. procainamide, procarbazine, metoclopramide, labetalol
  • A61K 31/497 - Non-condensed pyrazines containing further heterocyclic rings
  • A61K 31/4427 - Non-condensed pyridinesHydrogenated derivatives thereof containing further heterocyclic ring systems
  • A61K 31/444 - Non-condensed pyridinesHydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. amrinone
  • A61K 31/4436 - Non-condensed pyridinesHydrogenated derivatives thereof containing further heterocyclic ring systems containing a heterocyclic ring having sulfur as a ring hetero atom
  • A61K 31/4439 - Non-condensed pyridinesHydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
  • C07D 417/14 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group containing three or more hetero rings
  • C07C 233/69 - Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom of an acyclic saturated carbon skeleton
  • A61K 31/433 - Thiadiazoles

21.

3 and P2X⅔ receptor modulators for treatment of respiratory and gastrointestinal diseases

      
Application Number 13186078
Grant Number 08524725
Status In Force
Filing Date 2011-07-19
First Publication Date 2012-05-17
Grant Date 2013-09-03
Owner Roche Palo Alto LLC (USA)
Inventor
  • Broka, Chris Allen
  • Carter, David Scott
  • Dillon, Michael Patrick
  • Ford, Anthony P. D. W.
  • Hawley, Ronald Charles
  • Jahangir, Alam
  • Moore, Amy Geraldine
  • Parish, Daniel Warren

Abstract

2/3 receptor antagonist, the methods comprising administering to a subject in need thereof an effective amount of a compound of formula (I): 8 are as defined herein.

IPC Classes  ?

  • A61K 31/505 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim

22.

Triazole compounds II

      
Application Number 13287152
Grant Number 08697696
Status In Force
Filing Date 2011-11-02
First Publication Date 2012-05-10
Grant Date 2014-04-15
Owner Roche Palo Alto LLC (USA)
Inventor
  • Gabriel, Stephen Deems
  • Thomas, Andrew

Abstract

The present invention is concerned with novel triazole compounds of formula (I) 3 are as described herein, as well as pharmaceutically acceptable salts thereof. The compounds of present invention have affinity and selectivity for the GABA A α5 receptor. Further the present invention is concerned with the manufacture of the compounds of formula (I), pharmaceutical compositions comprising them and their use as pharmaceuticals.

IPC Classes  ?

  • C07D 403/12 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 405/14 - Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
  • C07D 413/14 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
  • C07D 417/06 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
  • C07D 417/14 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group containing three or more hetero rings

23.

Tetralin and indane derivatives and uses thereof

      
Application Number 13314525
Grant Number 08889906
Status In Force
Filing Date 2011-12-08
First Publication Date 2012-04-12
Grant Date 2014-11-18
Owner Roche Palo Alto LLC (USA)
Inventor
  • Greenhouse, Robert
  • Harris, Iii, Ralph New
  • Jaime-Figueroa, Saul
  • Kress, James M.
  • Repke, David Bruce
  • Stabler, Russell Stephen

Abstract

Compounds of the formula I: 2 are as defined herein. Also provided are methods for preparing, compositions comprising, and methods for using compounds of formula I.

IPC Classes  ?

  • C07C 303/00 - Preparation of esters or amides of sulfuric acidsPreparation of sulfonic acids or of their esters, halides, anhydrides or amides
  • C07C 307/00 - Amides of sulfuric acids, i.e. compounds having singly-bound oxygen atoms of sulfate groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
  • C07C 309/00 - Sulfonic acidsHalides, esters, or anhydrides thereof
  • C07C 311/00 - Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
  • A01N 47/28 - Ureas or thioureas containing the groups N—CO—N or N—CS—N
  • A61K 31/17 - Amides, e.g. hydroxamic acids having the group N—C(O)—N or N—C(S)—N, e.g. urea, thiourea, carmustine
  • A01N 37/18 - Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N, e.g. carboxylic acid amides or imidesThio-analogues thereof
  • A61K 31/16 - Amides, e.g. hydroxamic acids
  • C07D 207/36 - Oxygen or sulfur atoms
  • C07D 235/06 - BenzimidazolesHydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
  • C07D 233/34 - Ethylene-urea
  • C07D 209/30 - IndolesHydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
  • C07D 233/90 - Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
  • C07D 239/42 - One nitrogen atom
  • C07C 317/32 - SulfonesSulfoxides having sulfone or sulfoxide groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton with sulfone or sulfoxide groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
  • C07C 317/44 - SulfonesSulfoxides having sulfone or sulfoxide groups and carboxyl groups bound to the same carbon skeleton
  • C07D 233/48 - Nitrogen atoms not forming part of a nitro radical with acyclic hydrocarbon or substituted acyclic hydrocarbon radicals, attached to said nitrogen atoms
  • C07D 239/14 - Nitrogen atoms not forming part of a nitro radical with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, attached to said nitrogen atoms
  • C07D 207/325 - Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms with substituted hydrocarbon radicals directly attached to the ring nitrogen atom
  • C07D 233/88 - Nitrogen atoms, e.g. allantoin
  • C07D 207/16 - Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
  • C07D 233/84 - Sulfur atoms
  • C07D 233/54 - Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
  • C07D 207/34 - Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
  • C07D 233/64 - Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
  • C07D 231/18 - One oxygen or sulfur atom
  • C07D 233/20 - Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with substituted hydrocarbon radicals, directly attached to ring carbon atoms
  • C07D 277/82 - Nitrogen atoms

24.

2/3 antagonists

      
Application Number 13314529
Grant Number 08809402
Status In Force
Filing Date 2011-12-08
First Publication Date 2012-04-05
Grant Date 2014-08-19
Owner Roche Palo Alto LLC (USA)
Inventor
  • Chen, Li
  • Dillon, Michael Patrick
  • Feng, Lichun
  • Yang, Minmin

Abstract

Compounds of the formula I: 2/3 receptor antagonists and methods of making the compounds.

IPC Classes  ?

  • A61K 31/015 - Hydrocarbons carbocyclic
  • C07D 473/00 - Heterocyclic compounds containing purine ring systems
  • C07D 207/27 - 2-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms with substituted hydrocarbon radicals directly attached to the ring nitrogen atom
  • C07D 413/10 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
  • C07D 263/20 - Oxygen atoms attached in position 2
  • C07D 413/14 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
  • C07D 401/14 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
  • C07D 413/12 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 233/32 - One oxygen atom

25.

Heteroaryl pyrrolidinyl and piperidinyl ketone derivatives and uses thereof

      
Application Number 13301605
Grant Number 08513425
Status In Force
Filing Date 2011-11-21
First Publication Date 2012-03-15
Grant Date 2013-08-20
Owner Roche Palo Alto LLC (USA)
Inventor
  • Iyer, Pravin
  • Lin, Clara Jeou Jen
  • Lynch, Stephen M.
  • Lucas, Matthew C.
  • Madera, Ann Marie
  • Ozboya, Kerem Erol
  • Weikert, Robert James
  • Schoenfeld, Ryan Craig

Abstract

Compounds of the formula: b are defined herein. Also provided are pharmaceutical compositions, methods of using, and methods of preparing the compounds.

IPC Classes  ?

  • C07D 211/30 - Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by doubly bound oxygen or sulfur atoms or by two oxygen or sulfur atoms singly bound to the same carbon atom
  • A61K 31/445 - Non-condensed piperidines, e.g. piperocaine

26.

2/3 antagonists

      
Application Number 12843563
Grant Number 08501933
Status In Force
Filing Date 2010-07-26
First Publication Date 2012-01-26
Grant Date 2013-08-06
Owner Roche Palo Alto LLC (USA)
Inventor
  • Chen, Li
  • Dillon, Michael Patrick
  • Feng, Lichun
  • Hawley, Ronald Charles
  • Yang, Minmin

Abstract

Compounds of the formula I: 1 is a group of formula A or formula B, 2/3 receptor antagonist and methods of making the subject compounds.

IPC Classes  ?

  • C07D 345/00 - Heterocyclic compounds containing rings having selenium or tellurium atoms as the only ring hetero atoms
  • C07D 517/00 - Heterocyclic compounds containing in the condensed system at least one hetero ring having selenium, tellurium, or halogen atoms as ring hetero atoms

27.

2/3 antagonists

      
Application Number 13240249
Grant Number 08841336
Status In Force
Filing Date 2011-09-22
First Publication Date 2012-01-19
Grant Date 2014-09-23
Owner Roche Palo Alto LLC (USA)
Inventor
  • Chen, Li
  • Dillon, Michael Patrick
  • Feng, Lichun
  • Hawley, Ronald Charles
  • Yang, Minmin

Abstract

Compounds of the formula I: 2/3 receptor antagonist and methods of making the compounds.

IPC Classes  ?

  • A61K 31/41 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which is nitrogen, e.g. tetrazole
  • C07D 213/12 - Preparation by ring-closure involving the use of ammonia, amines, amine salts, or nitriles from unsaturated compounds
  • C07D 471/04 - Ortho-condensed systems
  • C07D 401/10 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing aromatic rings
  • C07D 405/12 - Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 257/04 - Five-membered rings
  • C07D 409/14 - Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
  • C07D 401/14 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings

28.

Quinoline inhibitors of hepatitis C virus polymerase

      
Application Number 13212742
Grant Number 08487103
Status In Force
Filing Date 2011-08-18
First Publication Date 2011-12-08
Grant Date 2013-07-16
Owner Roche Palo Alto LLC (USA)
Inventor
  • De Vicente Fidalgo, Javier
  • Li, Jim
  • Schoenfeld, Ryan Craig
  • Talamas, Francisco Xavier
  • Taygerly, Joshua Paul Gergely

Abstract

4 and as defined herein

IPC Classes  ?

  • C07D 215/00 - Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems

29.

Process for synthesis of phenoxy diaminopyrimidine derivatives

      
Application Number 13181305
Grant Number 08580960
Status In Force
Filing Date 2011-07-12
First Publication Date 2011-11-03
Grant Date 2013-11-12
Owner Roche Palo Alto LLC (USA)
Inventor
  • Dvorak, Charles Alois
  • Green, Keena Lynn
  • Lee, Gary R.

Abstract

A method for preparing a compound of formula k the method comprising treating a compound of formula j with ammonia, to form the compound of formula k.

IPC Classes  ?

30.

Triazole-substituted arylamides as P2X3 and P2X2/3 antagonists

      
Application Number 13162378
Grant Number 08440708
Status In Force
Filing Date 2011-06-16
First Publication Date 2011-10-06
Grant Date 2013-05-14
Owner Roche Palo Alto LLC (USA)
Inventor
  • Chen, Li
  • Dillon, Michael Patrick
  • Feng, Lichun
  • Hawley, Ronald Charles
  • Yang, Minmin

Abstract

Compounds of the formula I: 2/3 receptor antagonists and methods of making the compounds.

IPC Classes  ?

  • A61K 31/41 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which is nitrogen, e.g. tetrazole

31.

Heterocyclic antiviral compounds

      
Application Number 12709473
Grant Number 08293778
Status In Force
Filing Date 2010-02-20
First Publication Date 2011-08-25
Grant Date 2012-10-23
Owner Roche Palo Alto LLC (USA)
Inventor
  • Dunn, James Patrick
  • Elworthy, Todd Richard
  • Stefanidis, Dimitrios
  • Sweeney, Zachary Kevin

Abstract

5, are as defined herein.

IPC Classes  ?

  • A61K 31/44 - Non-condensed pyridinesHydrogenated derivatives thereof
  • A61K 31/427 - Thiazoles not condensed and containing further heterocyclic rings
  • A61K 31/4725 - Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
  • A61K 31/496 - Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
  • A61K 31/513 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim having oxo groups directly attached to the heterocyclic ring, e.g. cytosine
  • A61K 31/536 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and at least one oxygen as the ring hetero atoms, e.g. 1,2-oxazines ortho- or peri-condensed with carbocyclic ring systems
  • A61K 31/7068 - Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid
  • A61K 31/7072 - Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid having two oxo groups directly attached to the pyrimidine ring, e.g. uridine, uridylic acid, thymidine, zidovudine
  • A61K 31/708 - Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines containing purines, e.g. adenosine, adenylic acid having oxo groups directly attached to the purine ring system, e.g. guanosine, guanylic acid

32.

2/3 antagonists

      
Application Number 12820660
Grant Number 08093275
Status In Force
Filing Date 2010-06-22
First Publication Date 2010-12-23
Grant Date 2012-01-10
Owner Roche Palo Alto LLC (USA)
Inventor
  • Chen, Li
  • Dillon, Michael Patrick
  • Feng, Lichun
  • Yang, Minmin

Abstract

Compounds of the formula I: 2/3 receptor antagonists and methods of making the compounds.

IPC Classes  ?

  • A61K 31/44 - Non-condensed pyridinesHydrogenated derivatives thereof

33.

2/3 antagonists

      
Application Number 12820577
Grant Number 08283383
Status In Force
Filing Date 2010-06-22
First Publication Date 2010-12-23
Grant Date 2012-10-09
Owner Roche Palo Alto LLC (USA)
Inventor
  • Broka, Chris Allen
  • Hawley, Ronald Charles

Abstract

Compounds of the formula I: 2/3 receptor antagonists and methods of making the compounds.

IPC Classes  ?

34.

2/3 antagonists

      
Application Number 12820748
Grant Number 08476457
Status In Force
Filing Date 2010-06-22
First Publication Date 2010-12-23
Grant Date 2013-07-02
Owner Roche Palo Alto LLC (USA)
Inventor
  • Dillon, Michael Patrick
  • Krauss, Nancy Elisabeth

Abstract

Compounds of the formula I: 2/3 receptor antagonists and methods of making the compounds.

IPC Classes  ?

  • C07D 231/56 - BenzopyrazolesHydrogenated benzopyrazoles
  • C07D 213/26 - Radicals substituted by halogen atoms or nitro radicals
  • C07D 213/40 - Acylated substituent nitrogen atom
  • C07D 403/12 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 403/14 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group containing three or more hetero rings

35.

Pyridines

      
Application Number 12768762
Grant Number 08415379
Status In Force
Filing Date 2010-04-28
First Publication Date 2010-11-11
Grant Date 2013-04-09
Owner
  • Hoffmann-La Roche Inc. (USA)
  • Roche Palo Alto LLC (USA)
Inventor
  • Jakob-Roetne, Roland
  • Lucas, Matthew C.
  • Thomas, Andrew

Abstract

The present invention is concerned with isoxazole-pyridines of formula I, having affinity and selectivity for GABA A α5 receptor, their manufacture, pharmaceutical compositions containing them and their use as pharmaceuticals. The active compounds of the present invention are useful as cognitive enhancer or for the therapeutic and/or prophylactic treatment of cognitive disorders like Alzheimer's disease.

IPC Classes  ?

  • A61K 31/443 - Non-condensed pyridinesHydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with oxygen as a ring hetero atom
  • C07D 413/14 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings

36.

Pyridazines

      
Application Number 12768765
Grant Number 08410104
Status In Force
Filing Date 2010-04-28
First Publication Date 2010-11-11
Grant Date 2013-04-02
Owner
  • Hoffmann-La Roche Inc. (USA)
  • Roche Palo Alto LLC (USA)
Inventor
  • Lucas, Matthew C.
  • Thomas, Andrew

Abstract

The present invention is concerned with isoxazole-pyridazines of formula I, having affinity and selectivity for GABA A α5 receptor, their manufacture, pharmaceutical compositions containing them and their use as therapeutically active substances. The active compounds of the present invention are useful as cognitive enhancer or for the therapeutic and/or prophylactic treatment of cognitive disorders like Alzheimer's disease.

IPC Classes  ?

  • A61K 31/501 - PyridazinesHydrogenated pyridazines not condensed and containing further heterocyclic rings
  • C07D 413/12 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 413/14 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings

37.

Process for the preparation a ruthenium complex

      
Application Number 12775415
Grant Number 08288534
Status In Force
Filing Date 2010-05-06
First Publication Date 2010-11-11
Grant Date 2012-10-16
Owner Roche Palo Alto LLC (USA)
Inventor
  • Doppiu, Angelino
  • Karch, Ralf
  • Puentener, Kurt
  • Rivas-Nass, Andreas
  • Scalone, Michelangelo
  • Winde, Roland
  • Woerner, Eileen

Abstract

The invention relates to a novel process for the preparation of Ruthenium metathesis catalysts of the formula Ruthenium metathesis catalysts have been widely applied in the synthesis of macrocyclic drug compounds.

IPC Classes  ?

  • C07D 413/14 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
  • C07D 403/02 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group containing two hetero rings
  • C07D 209/48 - Iso-indolesHydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide
  • C07F 15/00 - Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table

38.

SYSTEMS AND METHODS FOR TAILORING ACUTE AND CHRONIC VIRAL INFECTION TREATMENTS TO INCREASE THE PROBABILITY OF "CURE" FOR A GIVEN SUBJECT

      
Application Number US2010033568
Publication Number 2010/129564
Status In Force
Filing Date 2010-05-04
Publication Date 2010-11-11
Owner ROCHE PALO ALTO LLC (USA)
Inventor
  • Snoeck, Eric
  • Chanu, Pascal, Francois
  • Goggin, Timothy
  • Jumbe, Nelson, L.
  • Frey, Nicolas

Abstract

In various embodiments, systems and methods are provided for increasing the likelihood of a sustained virological response or cure using a model of patient physiology incorporating a subjects race, gender, age, weight, concomitant medicines and disease state, immune response status, and responsiveness to drug therapies to simultaneously characterize the change in viral burden in the subject in terms of velocity of viral load decline. In an embodiment, once viral load in a subject is below a physical measurement limit, the model can extrapolate the subjects observed viral velocity toward a physiological target shown to be highly correlated with cure. In further embodiments, the model can be used for personalized medicine - the right drug at the right dose for the right treatment duration for the right patient. Accordingly, the model can provide optimal value for treatment and reducing the high cost of side effects.

IPC Classes  ?

  • G01N 33/48 - Biological material, e.g. blood, urineHaemocytometers
  • G01N 33/50 - Chemical analysis of biological material, e.g. blood, urineTesting involving biospecific ligand binding methodsImmunological testing

39.

Isoxazoles

      
Application Number 12766202
Grant Number 08227461
Status In Force
Filing Date 2010-04-23
First Publication Date 2010-11-04
Grant Date 2012-07-24
Owner ROCHE PALO ALTO LLC (USA)
Inventor
  • Jakob-Roetne, Roland
  • Lucas, Matthew C.
  • Thomas, Andrew

Abstract

The present invention is concerned with novel isoxazole derivatives of formula I 5 are as described herein, as well as pharmaceutically acceptable salts and esters thereof. The active compounds of the present invention have affinity and selectivity for GABA A α5 receptor. Further the present invention is concerned with the manufacture of the active compounds of formula I, pharmaceutical compositions containing them and their use as pharmaceuticals.

IPC Classes  ?

  • A61K 31/541 - Non-condensed thiazines containing further heterocyclic rings
  • A61K 31/5377 - 1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
  • A61K 31/4439 - Non-condensed pyridinesHydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
  • C07D 417/14 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group containing three or more hetero rings
  • C07D 413/14 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
  • C07D 401/12 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links

40.

Process for preparing triazolones

      
Application Number 12791252
Grant Number 07893276
Status In Force
Filing Date 2010-06-01
First Publication Date 2010-11-04
Grant Date 2011-02-22
Owner Roche Palo Alto LLC (USA)
Inventor
  • Lee, Gary M.
  • Zhu, Jiang

Abstract

The present process provides a improved method for the preparation of alkylsulfanyl substituted triazoles 2 which are useful intermediates in a new process for the preparation of triazolones 20.

IPC Classes  ?

41.

Stable cell lines expressing hERG

      
Application Number 12820358
Grant Number 08349572
Status In Force
Filing Date 2010-06-22
First Publication Date 2010-10-14
Grant Date 2013-01-08
Owner Roche Palo Alto LLC (USA)
Inventor
  • Dietrich, Paul Shartzer
  • Koch, Bruce
  • Guthrie, Heather
  • Gubler, Ulrich Andreas

Abstract

A stable eukaryotic cell line that expresses hERG and exhibits a stable current under electrophysiological test conditions is provided.

IPC Classes  ?

  • C12Q 1/00 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions

42.

Substituted isoxazoles

      
Application Number 12748524
Grant Number 08222246
Status In Force
Filing Date 2010-03-29
First Publication Date 2010-10-07
Grant Date 2012-07-17
Owner ROCHE PALO ALTO LLC (USA)
Inventor
  • Buettelmann, Bernd
  • Gabriel, Stephen Deems
  • Hanlon, Steven Paul
  • Jakob-Roetne, Roland
  • Lucas, Matthew C.
  • Spurr, Paul
  • Thomas, Andrew
  • Waldmeier, Pius

Abstract

The present invention is concerned with novel hydroxy-methyl isoxazole derivatives of formula I 3 are as described herein, as well as pharmaceutically acceptable salts and esters thereof. The active compounds of the present invention have affinity and selectivity for GABA A α5 receptor. Further the present invention is concerned with the manufacture of the active compounds of formula I, pharmaceutical compositions containing them and their use as pharmaceuticals.

IPC Classes  ?

  • C07D 413/02 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
  • A61K 31/44 - Non-condensed pyridinesHydrogenated derivatives thereof

43.

COMBINATION OF A NUCLEOSIDE POLYMERASE INHIBITOR WITH A MACROCYCLIC PROTEASE INHIBITOR AND USE THEREOF IN THE TREATMENT OF HEPATITIS C, LIVER FIBROSIS AND IMPAIRED LIVER FUNCTION

      
Application Number US2010025611
Publication Number 2010/099458
Status In Force
Filing Date 2010-02-26
Publication Date 2010-09-02
Owner
  • F. HOFFMANN-LA ROCHE LTD (Switzerland)
  • ROCHE PALO ALTO LLC (USA)
  • PHARMASSET, INC. (USA)
Inventor
  • Porter, Steven, B.
  • Bradford, Williamson, Ziegler
  • Smith, Patrick, F.
  • Yetzer, Ellen, S.
  • De La Rosa, Abel
  • Rogers, Michael, D.
  • Symonds, William, T.

Abstract

Embodiments disclosed in the present application relate to a composition that can include a hepatitis C viral polymerase inhibitor, or pharmaceutically acceptable salt or prodrug thereof and a hepatitis C viral protease inhibitor, or pharmaceutically acceptable salt or prodrug thereof. Additional embodiments disclosed relate to methods for treating a disease condition such as a hepatitis C virus infection, liver fibrosis and/or impaired liver function with a hepatitis C viral polymerase inhibitor, or pharmaceutically acceptable salt or prodrug thereof and a hepatitis C viral protease inhibitor, or pharmaceutically acceptable salt or prodrug thereof.

IPC Classes  ?

  • A61K 31/4709 - Non-condensed quinolines containing further heterocyclic rings
  • A61K 31/7068 - Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid
  • A61P 31/14 - Antivirals for RNA viruses
  • A61P 1/16 - Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics

44.

Thiadiazole-substituted arylamides as P2X3 and P2X2/3 antagonists

      
Application Number 12636723
Grant Number 08119644
Status In Force
Filing Date 2009-12-12
First Publication Date 2010-06-17
Grant Date 2012-02-21
Owner Roche Palo Alto LLP (USA)
Inventor
  • Chen, Li
  • Feng, Lichun
  • Yang, Minmin
  • Dillon, Michael Patrick
  • Lai, Yingjie

Abstract

Compounds of the formula I: 2/3 receptor antagonists and methods of making the compounds.

IPC Classes  ?

  • A61K 31/444 - Non-condensed pyridinesHydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. amrinone
  • A61K 31/497 - Non-condensed pyrazines containing further heterocyclic rings
  • A61K 31/433 - Thiadiazoles
  • A61P 13/00 - Drugs for disorders of the urinary system
  • A61P 13/10 - Drugs for disorders of the urinary system of the bladder
  • A61P 25/00 - Drugs for disorders of the nervous system
  • C07D 417/14 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group containing three or more hetero rings
  • C07D 285/06 - 1,2,3-ThiadiazolesHydrogenated 1,2,3-thiadiazoles

45.

Polymorphs of acyl sulfonamides

      
Application Number 12556235
Grant Number 08063103
Status In Force
Filing Date 2009-09-09
First Publication Date 2010-03-11
Grant Date 2011-11-22
Owner Roche Palo Alto LLC (USA)
Inventor
  • Davidson, James Prentice
  • Pang, Fei
  • Wong, Margaret
  • Martin, Michael

Abstract

The application discloses novel polymorphic crystalline forms of 2-[4-Bromo-3-(3-chloro-5-cyano-phenoxy)-2-fluoro-phenyl]-N-(2-chloro-4-propionylsulfamoyl-phenyl)-acetamide, sodium salt (Ib) with improved stability and physical properties which facilitate manufacturing, handling and formulating for treatment or prophylaxis of HIV mediated diseases, AIDS or ARC, in monotherapy or in combination therapy.

IPC Classes  ?

  • C07C 311/51 - Y being a hydrogen or a carbon atom
  • A61K 31/277 - NitrilesIsonitriles having a ring, e.g. verapamil

46.

Methods for treating retroviral infections

      
Application Number 12606320
Grant Number 08329755
Status In Force
Filing Date 2009-10-27
First Publication Date 2010-02-18
Grant Date 2012-12-11
Owner Roche Palo Alto LLC (USA)
Inventor
  • Dunn, James Patrick
  • Hirschfeld, Donald Roy
  • Silva, Tania
  • Sweeney, Zachary Kevin
  • Vora, Harit

Abstract

1 are as defined herein with at least one carrier, excipient or diluent.

IPC Classes  ?

  • A61K 31/16 - Amides, e.g. hydroxamic acids
  • A61K 31/165 - Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
  • A61K 31/18 - Sulfonamides

47.

PHOSPHODIESTERASE 4 INHIBITORS

      
Application Number US2009049558
Publication Number 2010/003084
Status In Force
Filing Date 2009-07-02
Publication Date 2010-01-07
Owner
  • MEMORY PHARMACEUTICALS CORPORATION (USA)
  • ROCHE PALO ALTO LLC (USA)
Inventor
  • Hopper, Allen, T.
  • Caroon, Joan, Marie
  • Chin, Elbert
  • Dunn, Robert
  • Labadie, Sharada, Shenvi
  • Li, Jim
  • Schumacher, Richard, Allen
  • Talamas, Francisco, Xavier

Abstract

PDE4 inhibition is achieved by novel compounds, e.g., N-substituted aniline and diphenylamine analogs. The compounds of the present invention are of Formula I: wherein R1, R2, R3, and R4 are as defined herein.

IPC Classes  ?

  • C07D 257/08 - Six-membered rings
  • A61K 31/395 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
  • A61K 31/41 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which is nitrogen, e.g. tetrazole
  • A61P 25/28 - Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia

48.

2/3 antagonists

      
Application Number 12583325
Grant Number 08193368
Status In Force
Filing Date 2009-08-18
First Publication Date 2009-12-31
Grant Date 2012-06-05
Owner Roche Palo Alto LLC (USA)
Inventor
  • Dillon, Michael Patrick
  • Hawley, Ronald Charles
  • Chen, Li
  • Feng, Lichun
  • Yang, Minmin

Abstract

Compounds of the formula I: 2/3 receptor antagonist and methods of making the compounds.

IPC Classes  ?

49.

Pyrazole-substituted arylamides as P2X3 and P2X2/3 antagonists

      
Application Number 12317008
Grant Number 08440673
Status In Force
Filing Date 2008-12-17
First Publication Date 2009-07-02
Grant Date 2013-05-14
Owner Roche Palo Alto LLC (USA)
Inventor
  • Chen, Li
  • Dillon, Michael Patrick
  • Feng, Lichun
  • Hawley, Ronald Charles
  • Yang, Minmin

Abstract

Compounds of the formula I: 2/3 receptor antagonists and methods of making the compounds.

IPC Classes  ?

  • A61K 31/4965 - Non-condensed pyrazines
  • A61K 31/415 - 1,2-Diazoles
  • C07D 231/00 - Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
  • C07D 401/14 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
  • C07D 221/00 - Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups

50.

2/3 antagonists

      
Application Number 12317026
Grant Number 08048905
Status In Force
Filing Date 2008-12-17
First Publication Date 2009-06-25
Grant Date 2011-11-01
Owner Roche Palo Alto LLC (USA)
Inventor
  • Chen, Li
  • Dillon, Michael Patrick
  • Feng, Lichun
  • Hawley, Ronald Charles
  • Yang, Minmin

Abstract

Compounds of the formula I: 2/3 receptor antagonist and methods of making the compounds.

IPC Classes  ?

  • A01N 43/64 - Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
  • A01N 33/02 - AminesQuaternary ammonium compounds
  • A61K 31/41 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which is nitrogen, e.g. tetrazole
  • A61K 31/13 - Amines, e.g. amantadine
  • C07D 257/04 - Five-membered rings

51.

Process for preparing triazolones

      
Application Number 12156145
Grant Number 07745634
Status In Force
Filing Date 2008-05-30
First Publication Date 2009-01-08
Grant Date 2010-06-29
Owner Roche Palo Alto LLC (USA)
Inventor
  • Arzeno, Humberto Bartolome
  • Lee, Gary M.
  • Martin, Michael
  • Sarma, Keshab
  • Zhu, Jiang

Abstract

The present process provides a improved method for the preparation of alkylsulfanyl substituted triazoles 2 which are useful intermediates in a new process for the preparation of triazolones 20.

IPC Classes  ?

52.

Pyrrolidinyl and piperidinyl ketone derivatives and uses thereof

      
Application Number 12002696
Grant Number 08084623
Status In Force
Filing Date 2007-12-18
First Publication Date 2008-06-19
Grant Date 2011-12-27
Owner Roche Palo Alto LLC (USA)
Inventor
  • Iyer, Pravin
  • Lin, Clara Jeou Jen
  • Lynch, Stephen M.
  • Lucas, Matthew C.
  • Madera, Ann Marie
  • Ozboya, Kerem Erol
  • Weikert, Robert James
  • Schoenfeld, Ryan Craig

Abstract

Compounds of the formula: b are defined herein. Also provided are pharmaceutical compositions, methods of using, and methods of preparing the compounds.

IPC Classes  ?

  • C07D 295/02 - Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements

53.

2/3 antagonists

      
Application Number 11983225
Grant Number 07786110
Status In Force
Filing Date 2007-11-08
First Publication Date 2008-06-05
Grant Date 2010-08-31
Owner Roche Palo Alto LLC (USA)
Inventor
  • Dillon, Michael Patrick
  • Hawley, Ronald Charles
  • Chen, Li
  • Feng, Lichun
  • Yang, Minmin

Abstract

Compounds of the formula I: 1 is a group of formula A or formula B, 2/3 receptor antagonist and methods of making the subject compounds.

IPC Classes  ?

  • C07D 417/12 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 277/30 - Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
  • C07D 263/32 - Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
  • C07D 413/12 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 277/66 - Benzothiazoles with only hydrocarbon or substituted hydrocarbon radicals attached in position 2 with aromatic rings or ring systems directly attached in position 2
  • A61K 31/497 - Non-condensed pyrazines containing further heterocyclic rings
  • A61K 31/5355 - Non-condensed oxazines containing further heterocyclic rings
  • A61K 31/428 - Thiazoles condensed with carbocyclic rings
  • A61K 31/426 - 1,3-Thiazoles
  • A61K 31/421 - 1,3-Oxazoles, e.g. pemoline, trimethadione
  • A61K 31/541 - Non-condensed thiazines containing further heterocyclic rings
  • A61P 13/00 - Drugs for disorders of the urinary system
  • A61P 11/00 - Drugs for disorders of the respiratory system
  • C07D 409/14 - Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
  • C07D 417/10 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a carbon chain containing aromatic rings

54.

Benzotriazole kinase modulators

      
Application Number 11899758
Grant Number 08962622
Status In Force
Filing Date 2007-09-07
First Publication Date 2008-05-01
Grant Date 2015-02-24
Owner Roche Palo Alto LLC (USA)
Inventor
  • Goldstein, David Michael
  • Gong, Levi
  • Michoud, Christophe
  • Palmer, Wylie Solang
  • Sidduri, Achyutharao

Abstract

Compounds of formula I modulate jnk and cdk: 3, and m are defined herein.

IPC Classes  ?

  • C07D 403/04 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group containing two hetero rings directly linked by a ring-member-to-ring- member bond
  • A61K 31/505 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim
  • C07D 403/14 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group containing three or more hetero rings

55.

Process for synthesis of phenoxy diaminopyrimidine derivatives

      
Application Number 11906802
Grant Number 08003788
Status In Force
Filing Date 2007-10-04
First Publication Date 2008-04-10
Grant Date 2011-08-23
Owner Roche Palo Alto LLC (USA)
Inventor
  • Dvorak, Charles Alois
  • Green, Keena Lynn
  • Lee, Gary R.

Abstract

A method for preparing a compound of formula k the method comprising treating a compound of formula j with ammonia, to form the compound of formula k.

IPC Classes  ?

  • C07D 239/48 - Two nitrogen atoms
  • C07C 43/20 - Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring

56.

2/3 antagonists

      
Application Number 11823808
Grant Number 07595405
Status In Force
Filing Date 2007-06-28
First Publication Date 2008-01-03
Grant Date 2009-09-29
Owner Roche Palo Alto LLC (USA)
Inventor
  • Dillon, Michael Patrick
  • Hawley, Ronald Charles
  • Chen, Li
  • Feng, Lichun
  • Yang, Minmin

Abstract

Compounds of the formula I: 2/3 receptor antagonist and methods of making the compounds.

IPC Classes  ?

57.

Stable cell lines expressing hERG

      
Application Number 11637511
Grant Number 07776590
Status In Force
Filing Date 2006-12-11
First Publication Date 2007-06-21
Grant Date 2010-08-17
Owner Roche Palo Alto LLC (USA)
Inventor
  • Dietrich, Paul Shartzer
  • Koch, Bruce
  • Guthrie, Heather
  • Gubler, Ulrich Andreas

Abstract

A stable eukaryotic cell line that expresses hERG and exhibits a stable current under electrophysiological test conditions is provided.

IPC Classes  ?

  • C12N 5/10 - Cells modified by introduction of foreign genetic material, e.g. virus-transformed cells
  • C12N 5/07 - Animal cells or tissues
  • C12N 5/00 - Undifferentiated human, animal or plant cells, e.g. cell linesTissuesCultivation or maintenance thereofCulture media therefor

58.

Method for the recombinant expression of a polypeptide

      
Application Number 11583573
Grant Number 07807409
Status In Force
Filing Date 2006-10-19
First Publication Date 2007-05-24
Grant Date 2010-10-05
Owner Roche Palo Alto LLC (USA)
Inventor Kopetzki, Erhard

Abstract

A method for the recombinant production of a heterologous polypeptide in a eukaryotic host cell is described. The host cell comprises an expression plasmid, whereby the expression plasmid comprises in a 5′ to 3′ direction a) a promoter, b) a nucleic acid encoding a first polypeptide, whose amino acid sequence is selected from Table 1 depending on the first two amino acids of the second polypeptide, c) a nucleic acid encoding a second polypeptide comprising a nucleic acid encoding a heterologous polypeptide, a nucleic acid encoding a linker, and a nucleic acid encoding an immunoglobulin fragment, and d) a 3′ untranslated region comprising a polyadenylation signal. Further a plasmid and a kit are described.

IPC Classes  ?

  • C12N 15/00 - Mutation or genetic engineeringDNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purificationUse of hosts therefor
  • C12N 15/63 - Introduction of foreign genetic material using vectorsVectorsUse of hosts thereforRegulation of expression

59.

2/3 modulators

      
Application Number 11509890
Grant Number 07799796
Status In Force
Filing Date 2006-08-25
First Publication Date 2007-03-01
Grant Date 2010-09-21
Owner Roche Palo Alto LLC (USA)
Inventor
  • Dillon, Michael Patrick
  • Jahangir, Alam
  • Lin, Clara Jeou Jen

Abstract

2/3 receptor antagonist, the compounds being of formula (I): 8 are as defined herein.

IPC Classes  ?

  • C07D 239/48 - Two nitrogen atoms
  • C07D 413/12 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
  • A61K 31/506 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings

60.

2/3 modulators

      
Application Number 11510216
Grant Number 07531547
Status In Force
Filing Date 2006-08-25
First Publication Date 2007-03-01
Grant Date 2009-05-12
Owner Roche Palo Alto LLC (USA)
Inventor
  • Dillon, Michael Patrick
  • Jahangir, Alam
  • Moore, Amy Geraldine
  • Wagner, Paul J.

Abstract

2/3 receptor antagonist, the methods comprising administering to a subject in need thereof an effective amount of a compound of formula (I): 8 are as defined herein.

IPC Classes  ?

61.

2/3 receptor modulators for treatment of respiratory and gastrointestinal diseases

      
Application Number 11509921
Grant Number 08008313
Status In Force
Filing Date 2006-08-25
First Publication Date 2007-03-01
Grant Date 2011-08-30
Owner Roche Palo Alto LLC (USA)
Inventor
  • Broka, Chris Allen
  • Carter, David Scott
  • Dillon, Michael Patrick
  • Ford, Anthony P. D. W.
  • Hawley, Ronald Charles
  • Jahangir, Alam
  • Moore, Amy Geraldine
  • Parish, Daniel Warren

Abstract

2/3 receptor antagonist, the methods comprising administering to a subject in need thereof an effective amount of a compound of formula (I): 8 are as defined herein.

IPC Classes  ?

  • A61K 31/505 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim

62.

2/3 modulators

      
Application Number 11510015
Grant Number 07776872
Status In Force
Filing Date 2006-08-25
First Publication Date 2007-03-01
Grant Date 2010-08-17
Owner Roche Palo Alto LLC (USA)
Inventor
  • Dillon, Michael Patrick
  • Jahangir, Alam
  • Lui, Alfred Sui-Ting
  • Wilhelm, Robert Stephen

Abstract

Compounds of the formula I: 2/3 receptor antagonist and methods of making the compounds.

IPC Classes  ?

  • C07D 239/48 - Two nitrogen atoms
  • C07D 401/12 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
  • A61K 31/506 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings

63.

Process for synthesis of phenoxy diaminopyrimidine derivatives

      
Application Number 11510208
Grant Number 07741484
Status In Force
Filing Date 2006-08-25
First Publication Date 2007-03-01
Grant Date 2010-06-22
Owner Roche Palo Alto LLC (USA)
Inventor
  • Constantinescu, Anton
  • Green, Keena Lynn
  • Humphreys, Eric Roy
  • Lee, Gary R.
  • Mcgarry, Patrick Finbar

Abstract

A method for preparing a compound of formula I the method comprising treating a compound of formula d 3 are as defined herein.

IPC Classes  ?

64.

3

      
Application Number 11502797
Grant Number 07491821
Status In Force
Filing Date 2006-08-11
First Publication Date 2007-02-15
Grant Date 2009-02-17
Owner Roche Palo Alto LLC (USA)
Inventor
  • Brotherton-Pleiss, Christine E.
  • Dillon, Michael Patrick
  • Gleason, Shelley K.
  • Lin, Clara Jeou Jen
  • Schoenfeld, Ryan Craig
  • Villa, Marzia
  • Zhai, Yansheng

Abstract

Compounds of formula 1 are modulators of P2X3 useful for the treatment of pain and genitourinary, gastrointestinal, and respiratory disorders: 1 is pyrimidin-2-yl, X is N, Y is a bond and A is oxazol-5-yl the carbon atom at position 4 in said oxazol-5-yl is not substituted by propyl when the carbon atom at position 2 in said oxazol-5-yl is substituted by substituted phenyl and the carbon atom at position 4 in said oxazol-5-yl is not substituted by phenyl when the carbon atom at position 2 is substituted by unsubstituted or substituted phenyl.

IPC Classes  ?

  • C07D 403/12 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 413/12 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 417/12 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 295/194 - Radicals derived from thio- or thiono carboxylic acids

65.

Tetralin and indane derivatives and uses thereof

      
Application Number 11315706
Grant Number 07312359
Status In Force
Filing Date 2005-12-21
First Publication Date 2006-07-27
Grant Date 2007-12-25
Owner Roche Palo Alto LLC (USA)
Inventor
  • Greenhouse, Robert
  • Harris, Iii, Ralph New
  • Jaime-Figueroa, Saul
  • Kress, James M.
  • Repke, David Bruce
  • Stabler, Russell Stephen

Abstract

Compounds of the formula I: 2 are as defined herein. Also provided are methods for preparing, compositions comprising, and methods for using compounds of formula I.

IPC Classes  ?

  • C07C 231/00 - Preparation of carboxylic acid amides
  • C07D 239/02 - Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
  • C07D 233/70 - One oxygen atom
  • A61K 31/50 - PyridazinesHydrogenated pyridazines
  • A61K 31/41 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which is nitrogen, e.g. tetrazole
  • A61K 31/17 - Amides, e.g. hydroxamic acids having the group N—C(O)—N or N—C(S)—N, e.g. urea, thiourea, carmustine
  • A61K 31/16 - Amides, e.g. hydroxamic acids

66.

Compositions and methods for treating cognitive disorders

      
Application Number 11241316
Grant Number 07713954
Status In Force
Filing Date 2005-11-14
First Publication Date 2006-03-30
Grant Date 2010-05-11
Owner Roche Palo Alto LLC (USA)
Inventor
  • Bonhaus, Douglas William
  • Martin, Renee Sharon

Abstract

Methods and pharmaceutical compositions relating to selective antagonists of the 5-HT6 receptor and 5-HT2A receptor useful for the treatment of cognitive disorders are presented.

IPC Classes  ?

  • A01N 43/00 - Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N 43/50 - 1,3-DiazolesHydrogenated 1,3-diazoles
  • A01N 41/10 - SulfonesSulfoxides
  • A61K 31/33 - Heterocyclic compounds
  • A61K 31/10 - SulfidesSulfoxidesSulfones
  • C07D 401/04 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring- member bond
  • C07D 471/04 - Ortho-condensed systems
  • C07D 487/04 - Ortho-condensed systems

67.

Heterocyclic antiviral compounds

      
Application Number 11190478
Grant Number 07666891
Status In Force
Filing Date 2005-07-27
First Publication Date 2006-02-02
Grant Date 2010-02-23
Owner Roche Palo Alto LLC (USA)
Inventor
  • Dunn, James Patrick
  • Elworthy, Todd Richard
  • Stefanidis, Dimitrios
  • Sweeney, Zachary Kevin

Abstract

5, are as defined herein.

IPC Classes  ?

  • A61K 31/44 - Non-condensed pyridinesHydrogenated derivatives thereof
  • C07D 249/12 - Oxygen or sulfur atoms

68.

Process for preparation of pyridine derivatives of NK-1 receptor antagonist

      
Application Number 11175799
Grant Number 07384939
Status In Force
Filing Date 2005-07-05
First Publication Date 2006-01-19
Grant Date 2008-06-10
Owner ROCHE PALO ALTO LLC (USA)
Inventor
  • Harrington, Peter J.
  • Johnston, David A.
  • Hodges, L. Mark

Abstract

The present invention provides a process for preparing a pyridine compound of the formula: 3 and a are those defined herein.

IPC Classes  ?

  • A61K 31/54 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and at least one sulfur as the ring hetero atoms, e.g. sulthiame
  • A61K 31/497 - Non-condensed pyrazines containing further heterocyclic rings
  • A61K 31/66 - Phosphorus compounds
  • C07D 279/10 - 1,4-ThiazinesHydrogenated 1,4-thiazines
  • C07D 401/00 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom

69.

Methods for treating retroviral infections

      
Application Number 11112590
Grant Number 07625949
Status In Force
Filing Date 2005-04-22
First Publication Date 2005-10-27
Grant Date 2009-12-01
Owner Roche Palo Alto LLC (USA)
Inventor
  • Dunn, James Patrick
  • Hirschfeld, Donald Roy
  • Silva, Tania
  • Sweeney, Zachary Kevin
  • Vora, Harit

Abstract

1 are as defined herein.

IPC Classes  ?

  • A61K 31/18 - Sulfonamides
  • A61K 31/165 - Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
  • A61K 31/33 - Heterocyclic compounds
  • A61K 31/497 - Non-condensed pyrazines containing further heterocyclic rings
  • A61K 31/435 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
  • A61K 31/44 - Non-condensed pyridinesHydrogenated derivatives thereof
  • A61K 31/40 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
  • A61K 31/405 - Indole-alkanecarboxylic acidsDerivatives thereof, e.g. tryptophan, indomethacin

70.

Non-nucleoside reverse transcriptase inhibitors

      
Application Number 11112591
Grant Number 07166738
Status In Force
Filing Date 2005-04-22
First Publication Date 2005-10-27
Grant Date 2007-01-23
Owner Roche Palo Alto LLC (USA)
Inventor
  • Dunn, James Patrick
  • Hirschfeld, Donald Roy
  • Silva, Tania
  • Sweeney, Zachary Kevin
  • Vora, Harit

Abstract

2 m, n, o and p are as defined herein

IPC Classes  ?

  • C07C 311/16 - Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom
  • C07C 311/17 - Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom to an acyclic carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms
  • C07C 311/18 - Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom to an acyclic carbon atom of a hydrocarbon radical substituted by nitrogen atoms, not being part of nitro or nitroso groups

71.

2/3 antagonists

      
Application Number 11071555
Grant Number 07858632
Status In Force
Filing Date 2005-03-03
First Publication Date 2005-09-22
Grant Date 2010-12-28
Owner Roche Palo Alto LLC (USA)
Inventor
  • Broka, Chris Allen
  • Carter, David Scott
  • Dillon, Michael Patrick
  • Hawley, Ronald Charles
  • Jahangir, Alam
  • Lin, Clara Jeou Jen
  • Parish, Daniel Warren

Abstract

2/3 receptor antagonist, the methods comprising administering to a subject in need thereof an effective amount of a compound of formula (I): 8 are as defined herein.

IPC Classes  ?

  • C07D 239/48 - Two nitrogen atoms
  • C07D 403/12 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a chain containing hetero atoms as chain links
  • A61K 31/505 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim

72.

Process and systems for peptide synthesis

      
Application Number 11021952
Grant Number 07439222
Status In Force
Filing Date 2004-12-23
First Publication Date 2005-07-28
Grant Date 2008-10-21
Owner ROCHE PALO ALTO LLC (USA)
Inventor
  • Guinn, Martin R.
  • Hodges, Lewis M.
  • Johnston, David A.
  • Moorlag, Hendrick
  • Schwindt, Mark A.

Abstract

The invention provides methods of synthesizing peptides, involving the steps of providing a composition including a peptide fragment, wherein the peptide fragment has at least one amino acid residue and includes a base-sensitive, N-terminal protecting group; removing the base-sensitive, N-terminal protecting group from the peptide fragment using a deprotection reagent that includes a base, whereby an N-terminal functionality on the peptide fragment is deprotected; removing the base from the composition to provide a residual base content of more than 100 ppm; causing a reactive peptide fragment having a reactive C-terminus and a base-sensitive N-terminal protecting group to react with the deprotected N-terminal functionality of the peptide fragment under conditions such that the reactive peptide fragment is added to the peptide fragment; and optionally repeating the deprotection and coupling steps until a desired peptide is obtained. Also provided are methods of synthesizing peptides, wherein base is removed from the composition to a point where the composition would provide a positive chloranil test. Also provided are methods of synthesizing peptides, wherein coupling is performed in basic reaction mixtures.

IPC Classes  ?

  • A01N 37/18 - Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N, e.g. carboxylic acid amides or imidesThio-analogues thereof
  • A61K 38/00 - Medicinal preparations containing peptides

73.

Non-nucleoside reverse transcriptase inhibitors

      
Application Number 10807766
Grant Number 07208509
Status In Force
Filing Date 2004-03-23
First Publication Date 2004-09-30
Grant Date 2007-04-24
Owner Roche Palo Alto LLC (USA)
Inventor
  • Dunn, James Patrick
  • Swallow, Steven
  • Sweeney, Zachary Kevin

Abstract

2 are as defined in the summary and pharmaceutically acceptable salts and solvates thereof, methods to inhibit or modulate Human Immunodeficiency Virus (HIV) reverse transcriptase with compounds of formula I, pharmaceutical compositions containing of formula I admixed with at least one solvent, carrier or excipient and processes to prepare compounds of formula I. The compounds are useful for treating disorders in which HIV and genetically related viruses are implicated

IPC Classes  ?

  • A61K 31/433 - Thiadiazoles
  • A61K 31/4245 - Oxadiazoles
  • A61K 31/4196 - 1,2,4-Triazoles
  • C07D 285/13 - Oxygen atoms
  • C07D 249/12 - Oxygen or sulfur atoms
  • C07D 271/113 - 1,3,4-OxadiazolesHydrogenated 1,3,4-oxadiazoles with oxygen, sulfur or nitrogen atoms, directly attached to ring carbon atoms, the nitrogen atoms not forming part of a nitro radical

74.

Methods for increasing bone formation using inhibitors of glycogen synthase kinase-3β

      
Application Number 10339193
Grant Number 07476676
Status In Force
Filing Date 2003-01-09
First Publication Date 2003-09-18
Grant Date 2009-01-13
Owner Roche Palo Alto LLC (USA)
Inventor
  • Day-Lollini, Patricia Ann
  • Gong, Leyi

Abstract

This invention relates to the use of inhibitors of glycogen synthase kinase-3β to increase bone formation.

IPC Classes  ?

  • C07D 471/04 - Ortho-condensed systems
  • A01N 43/42 - Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings condensed with carbocyclic rings
  • A01N 43/38 - Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings condensed with carbocyclic rings