IN2013CN09764A - - Google Patents
Info
- Publication number
- IN2013CN09764A IN2013CN09764A IN9764CHN2013A IN2013CN09764A IN 2013CN09764 A IN2013CN09764 A IN 2013CN09764A IN 9764CHN2013 A IN9764CHN2013 A IN 9764CHN2013A IN 2013CN09764 A IN2013CN09764 A IN 2013CN09764A
- Authority
- IN
- India
- Prior art keywords
- alkyl
- hydrogen
- formula
- alkylheterocyclylalkyl
- ch2cn
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Medicinal Chemistry (AREA)
- Psychiatry (AREA)
- Neurology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Biomedical Technology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Neurosurgery (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
A compound of formula (I) pharmaceutical^ acceptable salt thereof, wherein Rl is selected from hydrogen, Ci-C6 alkyl; Ci-C6 alkyl(C3-C8)cycloalkyl; Ci- C6 hydroxyalkyl; CH2CN; CH2C(0)NH2; Ci-C6 arylalkyl; and Ci-C6 10 alkylheterocyclylalkyl; R'-R° are independently selected from hydrogen, Ci-Ce alkoxy; and halo; and 7 R is a heteroaromatic group of formula (II) containing from 2 to 4 nitrogen atoms: Y^Z C3I6>
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201161499360P | 2011-06-21 | 2011-06-21 | |
PCT/US2012/043310 WO2012177738A1 (en) | 2011-06-21 | 2012-06-20 | Imidazole derivatives as inhibitors of pde10 |
Publications (1)
Publication Number | Publication Date |
---|---|
IN2013CN09764A true IN2013CN09764A (en) | 2015-04-03 |
Family
ID=46420554
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
IN9764CHN2013 IN2013CN09764A (en) | 2011-06-21 | 2012-06-20 |
Country Status (3)
Country | Link |
---|---|
US (1) | US8592423B2 (en) |
IN (1) | IN2013CN09764A (en) |
WO (1) | WO2012177738A1 (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2861596B1 (en) * | 2012-06-19 | 2019-03-20 | Sunovion Pharmaceuticals Inc. | Heteroaryl compounds and methods of use thereof |
ES2480341B1 (en) | 2013-01-24 | 2015-01-22 | Palobiofarma S.L | New derivatives of pyrimidine as phosphodiesterase 10 (PDE-10) inhibitors |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
PT100905A (en) | 1991-09-30 | 1994-02-28 | Eisai Co Ltd | BICYCLE HYGIENEOUS HETEROCYCLIC COMPOUNDS CONTAINING BENZENE, CYCLOHEXAN OR PYRIDINE AND PYRIMIDINE, PYRIDINE OR IMIDAZOLE SUBSTITUTES AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM |
US20030032579A1 (en) | 2001-04-20 | 2003-02-13 | Pfizer Inc. | Therapeutic use of selective PDE10 inhibitors |
CN1894241A (en) | 2002-08-09 | 2007-01-10 | 阿斯利康(瑞典)有限公司 | '1,2,4' oxadiazoles as modulators of metabotropic glutamate receptor-5 |
CN1805945A (en) | 2003-04-18 | 2006-07-19 | 麦克公司 | Biaryl substituted thiazoles, oxazoles and imidazoles as sodium channel blockers |
EP1741708A1 (en) | 2005-06-28 | 2007-01-10 | Sanofi-Aventis Deutschland GmbH | Heteroaryl-substituted amides comprising an unsaturated or cyclic linker group, and their use as pharmaceuticals |
US8133897B2 (en) | 2008-06-20 | 2012-03-13 | H. Lundbeck A/S | Phenylimidazole derivatives as PDE10A enzyme inhibitors |
TW201200516A (en) | 2009-12-17 | 2012-01-01 | Lundbeck & Co As H | Phenylimidazole derivatives comprising an ethynylene linker as PDE10A enzyme inhibitors |
AR080754A1 (en) | 2010-03-09 | 2012-05-09 | Janssen Pharmaceutica Nv | IMIDAZO DERIVATIVES (1,2-A) PIRAZINA AND ITS USE AS PDE10 INHIBITORS |
-
2012
- 2012-06-18 US US13/525,976 patent/US8592423B2/en active Active
- 2012-06-20 IN IN9764CHN2013 patent/IN2013CN09764A/en unknown
- 2012-06-20 WO PCT/US2012/043310 patent/WO2012177738A1/en unknown
Also Published As
Publication number | Publication date |
---|---|
US8592423B2 (en) | 2013-11-26 |
US20130150371A1 (en) | 2013-06-13 |
WO2012177738A1 (en) | 2012-12-27 |
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