MA35274B1 - Cristal de composé hétérocyclique condensé - Google Patents
Cristal de composé hétérocyclique condenséInfo
- Publication number
- MA35274B1 MA35274B1 MA36695A MA36695A MA35274B1 MA 35274 B1 MA35274 B1 MA 35274B1 MA 36695 A MA36695 A MA 36695A MA 36695 A MA36695 A MA 36695A MA 35274 B1 MA35274 B1 MA 35274B1
- Authority
- MA
- Morocco
- Prior art keywords
- heterocyclic compound
- condensed heterocyclic
- compound crystal
- crystal
- imidazo
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Psychiatry (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Crystals, And After-Treatments Of Crystals (AREA)
Abstract
La présente invention concerne un cristal de 1-éthyl-7-méthyl-3-{4-[(3- méthyl-3h-imidazo[4,5-b]pyridin-2-yl)oxy]phényl}-1,3-dihydro-2h- imidazo[4,5-b]pyridin-2-one utile en tant qu'agent prophylactique ou thérapeutique pour la schizophrénie et analogues, ledit cristal présentant un profil de diffraction des rayons x sur poudre affichant des pics caractéristiques à des distances interplanaires (d) de 13,59 plus ou moins 0,2 et de 6,76 plus ou moins 0,2 angströms dans la diffraction des rayons x sur poudre
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2011138920 | 2011-06-22 | ||
PCT/JP2012/066461 WO2012176934A1 (fr) | 2011-06-22 | 2012-06-21 | Cristal de composé hétérocyclique condensé |
Publications (1)
Publication Number | Publication Date |
---|---|
MA35274B1 true MA35274B1 (fr) | 2014-07-03 |
Family
ID=46551819
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MA36695A MA35274B1 (fr) | 2011-06-22 | 2014-01-20 | Cristal de composé hétérocyclique condensé |
Country Status (26)
Country | Link |
---|---|
US (1) | US9512118B2 (fr) |
EP (1) | EP2723738B1 (fr) |
JP (1) | JP6025757B2 (fr) |
KR (1) | KR20140040777A (fr) |
CN (1) | CN103608348B (fr) |
AR (1) | AR087004A1 (fr) |
AU (1) | AU2012274292B2 (fr) |
BR (1) | BR112013032052A2 (fr) |
CA (1) | CA2839825C (fr) |
CL (1) | CL2013003632A1 (fr) |
CO (1) | CO6862150A2 (fr) |
CR (1) | CR20140033A (fr) |
DO (1) | DOP2013000311A (fr) |
EA (1) | EA026137B1 (fr) |
EC (1) | ECSP14013165A (fr) |
GE (1) | GEP20166475B (fr) |
MA (1) | MA35274B1 (fr) |
MX (1) | MX342990B (fr) |
MY (1) | MY163483A (fr) |
PE (1) | PE20141030A1 (fr) |
TN (1) | TN2013000510A1 (fr) |
TW (1) | TWI570122B (fr) |
UA (1) | UA112082C2 (fr) |
UY (1) | UY34150A (fr) |
WO (1) | WO2012176934A1 (fr) |
ZA (1) | ZA201309611B (fr) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5973990B2 (ja) * | 2011-03-16 | 2016-08-23 | 武田薬品工業株式会社 | 縮合複素環化合物 |
US10851076B2 (en) | 2017-08-10 | 2020-12-01 | Pratt Bethers | Method for purifying crystals using solvent vapors |
US10960322B2 (en) | 2018-07-02 | 2021-03-30 | Pratt Bethers | Apparatus for purifying crystals using solvent vapors |
US10308626B1 (en) | 2018-07-02 | 2019-06-04 | Pratt Bethers | Crystal purification in a glass or metal container |
US20240052227A1 (en) * | 2022-08-12 | 2024-02-15 | Raytheon Company | Water-based polymer network for transpirant cooling applications |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5597826A (en) * | 1994-09-14 | 1997-01-28 | Pfizer Inc. | Compositions containing sertraline and a 5-HT1D receptor agonist or antagonist |
CA2582479C (fr) * | 2004-10-07 | 2011-07-12 | Pfizer Products Inc. | Derives de benzoimidazole utiles en tant qu'agents antiproliferatifs |
AU2006285915B2 (en) | 2005-08-30 | 2011-02-24 | Asahi Kasei Pharma Corporation | Sulfonamide compound |
FI20055498A0 (fi) | 2005-09-16 | 2005-09-16 | Biotie Therapies Corp | Sulfonamidijohdannaisia |
US7618982B2 (en) | 2005-12-19 | 2009-11-17 | Nerviano Medical Sciences S.R.L. | Heteroarylpyrrolopyridinones active as kinase inhibitors |
CN101384583A (zh) * | 2006-02-15 | 2009-03-11 | 塞诺菲-安万特股份有限公司 | 氮杂环基-取代的芳基二氢异喹啉酮、它们的制备方法和它们作为药物的用途 |
US20080090834A1 (en) | 2006-07-06 | 2008-04-17 | Pfizer Inc | Selective azole pde10a inhibitor compounds |
JP5313883B2 (ja) | 2007-04-18 | 2013-10-09 | キッセイ薬品工業株式会社 | 含窒素縮合環誘導体、それを含有する医薬組成物及びその医薬用途 |
CA2717529A1 (fr) | 2008-03-11 | 2009-09-17 | Cellzome Limited | Sulfonamides en tant qu'inhibiteurs de zap-70 |
TW201030001A (en) | 2008-11-14 | 2010-08-16 | Amgen Inc | Pyridine and pyrimidine derivatives as phosphodiesterase 10 inhibitors |
TWI396689B (zh) | 2008-11-14 | 2013-05-21 | Amgen Inc | 作為磷酸二酯酶10抑制劑之吡衍生物 |
WO2010126002A1 (fr) | 2009-04-28 | 2010-11-04 | 塩野義製薬株式会社 | Produit pharmaceutique contenant un composé sulfonamide hétérocyclique |
MY165585A (en) | 2010-06-24 | 2018-04-05 | Takeda Pharmaceuticals Co | Fused heterocyclic compounds as phosphodiesterases (pdes) inhibitors |
US9029536B2 (en) | 2010-08-04 | 2015-05-12 | Takeda Pharmaceutical Company Limited | Fused heterocyclic compounds |
EP2604597B1 (fr) | 2010-08-10 | 2017-01-04 | Takeda Pharmaceutical Company Limited | Composé hétérocyclique et utilisation de celui-ci comme inhibiteur de phosphodiesterase 10a |
JP5973990B2 (ja) | 2011-03-16 | 2016-08-23 | 武田薬品工業株式会社 | 縮合複素環化合物 |
-
2012
- 2012-06-20 TW TW101122358A patent/TWI570122B/zh not_active IP Right Cessation
- 2012-06-21 EP EP12738230.7A patent/EP2723738B1/fr active Active
- 2012-06-21 MX MX2013015354A patent/MX342990B/es active IP Right Grant
- 2012-06-21 UY UY0001034150A patent/UY34150A/es not_active Application Discontinuation
- 2012-06-21 AR ARP120102205A patent/AR087004A1/es unknown
- 2012-06-21 UA UAA201400581A patent/UA112082C2/uk unknown
- 2012-06-21 KR KR1020137034952A patent/KR20140040777A/ko not_active Application Discontinuation
- 2012-06-21 CN CN201280029988.3A patent/CN103608348B/zh active Active
- 2012-06-21 GE GEAP201213352A patent/GEP20166475B/en unknown
- 2012-06-21 CA CA2839825A patent/CA2839825C/fr not_active Expired - Fee Related
- 2012-06-21 BR BR112013032052A patent/BR112013032052A2/pt not_active IP Right Cessation
- 2012-06-21 US US14/125,390 patent/US9512118B2/en active Active
- 2012-06-21 MY MYPI2013004544A patent/MY163483A/en unknown
- 2012-06-21 PE PE2013002859A patent/PE20141030A1/es not_active Application Discontinuation
- 2012-06-21 EA EA201490092A patent/EA026137B1/ru not_active IP Right Cessation
- 2012-06-21 WO PCT/JP2012/066461 patent/WO2012176934A1/fr active Application Filing
- 2012-06-21 JP JP2013557956A patent/JP6025757B2/ja active Active
- 2012-06-21 AU AU2012274292A patent/AU2012274292B2/en not_active Ceased
-
2013
- 2013-12-06 TN TNP2013000510A patent/TN2013000510A1/fr unknown
- 2013-12-18 CL CL2013003632A patent/CL2013003632A1/es unknown
- 2013-12-19 ZA ZA2013/09611A patent/ZA201309611B/en unknown
- 2013-12-20 DO DO2013000311A patent/DOP2013000311A/es unknown
-
2014
- 2014-01-20 MA MA36695A patent/MA35274B1/fr unknown
- 2014-01-21 CO CO14010660A patent/CO6862150A2/es not_active Application Discontinuation
- 2014-01-22 EC ECSP14013165 patent/ECSP14013165A/es unknown
- 2014-01-22 CR CR20140033A patent/CR20140033A/es unknown
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
MA35274B1 (fr) | Cristal de composé hétérocyclique condensé | |
MA35452B1 (fr) | 3-pyrimidin-4-yl-oxazolidin-2-ones comme inhibiteurs d'idh mutante | |
MX347562B (es) | Derivados fungicidas de 3-fenil[(heterociclilmetoxi)imino]metil}-1 ,2,4-oxadiazol-5(4h)-ona sustituidos en 4. | |
WO2007034282A3 (fr) | Composes de biphenylimidazole utilises comme antagonistes du recepteur du c3a | |
RS53828B1 (en) | CONCLUSION OF IMIDASO [4,5-C] HINOLIN-2-ON AND ITS USE AS A DOUBLE P13 KINASE / mTOR INHIBITOR | |
SG195289A1 (en) | Process for preparing heterocyclic compounds including trans-7-oxo-6-(sulphooxy)-1,6-diazabicyclo[3,2,1]octane-2-carboxamide and salts thereof | |
MX2019010100A (es) | Compuesto de quinolona. | |
WO2008032157A3 (fr) | Synthèse de 2-(pyridin-2-ylamino)-pyrido[2,3-d]pyrimidin-7-ones | |
NZ605889A (en) | Fused heterocyclic compounds as phosphodiesterases (pdes) inhibitors | |
MX2010008469A (es) | Pirazolopirimidinas, procedimiento para su preparacion y su uso como medicina. | |
WO2008050168A8 (fr) | Nouveaux dérivés sulfonamides utilisés comme antagonistes de la bradykinine | |
MX2013001805A (es) | Derivados de 2-(arilamino)-3h-imidazo [4,5-b] piridina-6-carboxamida y su uso como inhibidores de mpges-1. | |
WO2014009833A3 (fr) | Modulateurs de trajet de complément et leurs utilisations | |
WO2008104175A3 (fr) | Nouveaux inhibiteurs de la phosphodiestérase | |
NO20080033L (no) | Kinolinderivater som NK3-antagonister | |
MX337638B (es) | Isoxazolo [5, 4-b] piridinas herbicidas. | |
WO2008136378A1 (fr) | Nouveau dérivé de sulfonamide et son sel | |
ATE514698T1 (de) | Tetracyclische azapyrazinoindoline als 5-ht2- liganden | |
WO2013106756A3 (fr) | Agents antimicrobiens | |
HU0700756D0 (en) | Process for producing pharmaceutical intermediers | |
MY161831A (en) | New non-peptide derivatives as bradykinin b1 antagonists | |
MX2012012531A (es) | Derivado de imidazo [1, 2-a] piridina. | |
WO2012035171A3 (fr) | Nouveaux composés | |
SG166799A1 (en) | Quinoline derivatives as antibacterial agents | |
MX2015005884A (es) | Compuesto de 2-piridona. |