AR056560A1 - Pirrolopiridinonas como moduladores cb1 - Google Patents
Pirrolopiridinonas como moduladores cb1Info
- Publication number
- AR056560A1 AR056560A1 ARP060104347A ARP060104347A AR056560A1 AR 056560 A1 AR056560 A1 AR 056560A1 AR P060104347 A ARP060104347 A AR P060104347A AR P060104347 A ARP060104347 A AR P060104347A AR 056560 A1 AR056560 A1 AR 056560A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl group
- group
- hydroxy
- compounds
- substituted
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 abstract 3
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- 229910003827 NRaRb Inorganic materials 0.000 abstract 1
- 208000012902 Nervous system disease Diseases 0.000 abstract 1
- 208000025966 Neurological disease Diseases 0.000 abstract 1
- 208000008589 Obesity Diseases 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 235000020824 obesity Nutrition 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 abstract 1
- 208000020016 psychiatric disease Diseases 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 230000001225 therapeutic effect Effects 0.000 abstract 1
Classifications
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- 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
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- 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
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- Urology & Nephrology (AREA)
Abstract
Procesos para la preparacion de dichos compuestos; con su uso en el tratamiento de obesidad, trastornos psiquiátricos y neurologicos; con métodos para su uso terapéutico; y con composiciones farmacéuticas que contienen dichos compuestos. Reivindicacion 1: Un compuesto de la formula (1) donde R1 representa un grupo alquilo C3-7 sustituido con uno o más F; o R1 representa un grupo alquilsulfonilo C1-7 sustituido con uno o más F; R2 representa ciano, o un grupo alquilo C1- 4 opcionalmente sustituido con hidroxi o con un grupo NRaRb, en el cual Ra y Rb representan de manera independiente H o un grupo alquilo C1-3; R3 representa piperidin-1-ilo o ciclohexilo, cada uno de los cuales está opcionalmente sustituido con uno o más grupos seleccionados de hidroxi, F o un grupo NRcRd en el cual Rc y Rd representan de manera independiente H o un grupo alquilo C1-3; y ---- es un enlace adicional opcional entre las posiciones 6 y 7; R4 representa Cl, F, ciano o metilo; n es 1, 2 o 3, y cada R4 se selecciona de modo independiente cuando n > 1; y sus sales aceptables para uso farmacéutico
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US72415605P | 2005-10-06 | 2005-10-06 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR056560A1 true AR056560A1 (es) | 2007-10-10 |
Family
ID=37781800
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP060104347A AR056560A1 (es) | 2005-10-06 | 2006-10-03 | Pirrolopiridinonas como moduladores cb1 |
Country Status (20)
| Country | Link |
|---|---|
| US (2) | US7875626B2 (es) |
| EP (1) | EP1937679B1 (es) |
| JP (1) | JP4277062B2 (es) |
| KR (1) | KR20080058456A (es) |
| CN (1) | CN101277957A (es) |
| AR (1) | AR056560A1 (es) |
| AT (1) | ATE440099T1 (es) |
| AU (1) | AU2006298530B2 (es) |
| BR (1) | BRPI0616653A2 (es) |
| CA (1) | CA2624495A1 (es) |
| DE (1) | DE602006008641D1 (es) |
| EC (1) | ECSP088413A (es) |
| ES (1) | ES2329616T3 (es) |
| IL (1) | IL190025A0 (es) |
| NO (1) | NO20081523L (es) |
| RU (1) | RU2415856C2 (es) |
| TW (1) | TW200730525A (es) |
| UY (1) | UY29838A1 (es) |
| WO (1) | WO2007039740A2 (es) |
| ZA (1) | ZA200802946B (es) |
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| AR056560A1 (es) * | 2005-10-06 | 2007-10-10 | Astrazeneca Ab | Pirrolopiridinonas como moduladores cb1 |
| JP5256047B2 (ja) * | 2006-01-27 | 2013-08-07 | シャンハイ ヘンルイ ファーマシューティカル カンパニー リミテッド | ピロロ[3,2−c]ピリジン−4−オン2−インドリノン(indolinone)プロテインキナーゼ阻害剤 |
| AU2007283113A1 (en) | 2006-08-08 | 2008-02-14 | Sanofi-Aventis | Arylaminoaryl-alkyl-substituted imidazolidine-2,4-diones, processes for preparing them, medicaments comprising these compounds, and their use |
| AR065909A1 (es) * | 2007-04-03 | 2009-07-08 | Astrazeneca Ab | Agentes terapeuticos 685 |
| EP2025674A1 (de) | 2007-08-15 | 2009-02-18 | sanofi-aventis | Substituierte Tetrahydronaphthaline, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
| EP2247588B1 (en) * | 2008-02-26 | 2016-04-13 | Takeda Pharmaceutical Company Limited | Fused heterocyclic derivative and use thereof |
| EP2310372B1 (en) | 2008-07-09 | 2012-05-23 | Sanofi | Heterocyclic compounds, processes for their preparation, medicaments comprising these compounds, and the use thereof |
| WO2010068601A1 (en) | 2008-12-08 | 2010-06-17 | Sanofi-Aventis | A crystalline heteroaromatic fluoroglycoside hydrate, processes for making, methods of use and pharmaceutical compositions thereof |
| US20110015154A1 (en) * | 2009-07-20 | 2011-01-20 | Kellermann Gottfried H | Supporting acetylcholine function |
| ES2443016T3 (es) | 2009-08-26 | 2014-02-17 | Sanofi | Nuevos hidratos cristalinos de fluoroglicósidos heteroaromáticos, productos farmacéuticos que comprenden estos compuestos, y su empleo |
| US20110098265A1 (en) * | 2009-10-28 | 2011-04-28 | Neuroscience, Inc. | Methods for reducing cravings and impulses associated with addictive and compulsive behaviors |
| EP2582709B1 (de) | 2010-06-18 | 2018-01-24 | Sanofi | Azolopyridin-3-on-derivate als inhibitoren von lipasen und phospholipasen |
| KR101273643B1 (ko) * | 2010-10-12 | 2013-06-11 | 한국화학연구원 | 5,6-디하이드로-피롤로[3,4-b]피리딘-7-온 유도체 또는 이의 약학적으로 허용 가능한 염, 이의 제조방법 및 이를 유효성분으로 포함하는 약학적 조성물 |
| US8828995B2 (en) | 2011-03-08 | 2014-09-09 | Sanofi | Branched oxathiazine derivatives, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof |
| EP2683705B1 (de) | 2011-03-08 | 2015-04-22 | Sanofi | Di- und trisubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
| EP2683699B1 (de) | 2011-03-08 | 2015-06-24 | Sanofi | Di- und trisubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
| EP2766349B1 (de) | 2011-03-08 | 2016-06-01 | Sanofi | Mit carbozyklen oder heterozyklen substituierte oxathiazinderivate, verfahren zu deren herstellung, diese verbindungen enthaltende arzneimittel und deren verwendung |
| EP2683700B1 (de) | 2011-03-08 | 2015-02-18 | Sanofi | Tetrasubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
| US9560630B2 (en) * | 2011-08-12 | 2017-01-31 | Qualcomm Incorporated | Devices for reduced overhead paging |
| HRP20200253T1 (hr) | 2013-03-06 | 2020-05-29 | Janssen Pharmaceutica Nv | Benzoimidazol-2-il pirimidinski modulatori histaminskog h4 receptora |
| MX380239B (es) | 2015-01-28 | 2025-03-12 | Bayer Pharma AG | Derivados de 4h-pirrol[3,2-c]piridin-4-ona. |
| WO2020074403A1 (en) * | 2018-10-08 | 2020-04-16 | Universität Zürich | Appetite-modulating molecules |
| WO2020161257A1 (en) | 2019-02-07 | 2020-08-13 | Bayer Aktiengesellschaft | 3-amino-2-[2-(acylamino)pyridin-4-yl]-1,5,6,7-tetrahydro-4h-pyrrolo[3,2-c]pyridin-4-one as csnk1 inhibitors |
| US20210015762A1 (en) * | 2019-07-16 | 2021-01-21 | TRUETIVA, Inc. | Compositions for treating obesity |
| KR20210103688A (ko) | 2020-02-14 | 2021-08-24 | (주) 디엔테크 | 오링용 고무조성물 |
| WO2022023337A1 (en) | 2020-07-29 | 2022-02-03 | Bayer Aktiengesellschaft | Substituted pyrrolo-pyridinone derivatives and therapeutic uses thereof |
| US20230322767A1 (en) | 2020-07-29 | 2023-10-12 | Bayer Aktiengesellschaft | Aryl substituted pyrrolo-pyridinones and therapeutic uses thereof |
| CN115108895A (zh) * | 2022-07-06 | 2022-09-27 | 四川东材科技集团成都新材料有限公司 | 一种1-(1-乙氧基乙氧基)-4-乙烯基苯的合成方法 |
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| FR2692575B1 (fr) | 1992-06-23 | 1995-06-30 | Sanofi Elf | Nouveaux derives du pyrazole, procede pour leur preparation et compositions pharmaceutiques les contenant. |
| US5451566A (en) * | 1993-11-17 | 1995-09-19 | Zeneca Limited | Herbicidal pyrrolopyridine compounds |
| FR2714057B1 (fr) | 1993-12-17 | 1996-03-08 | Sanofi Elf | Nouveaux dérivés du 3-pyrazolecarboxamide, procédé pour leur préparation et compositions pharmaceutiques les contenant. |
| FR2758723B1 (fr) | 1997-01-28 | 1999-04-23 | Sanofi Sa | Utilisation des antagonistes des recepteurs aux cannabinoides centraux pour la preparation de medicaments |
| US6858616B2 (en) | 1998-12-23 | 2005-02-22 | Bristol-Myers Squibb Pharma Company | Nitrogen containing heterobicycles as factor Xa inhibitors |
| CN1205188C (zh) | 2000-03-23 | 2005-06-08 | 索尔瓦药物有限公司 | 具有cb1-拮抗活性的4,5-二氢-1h-吡唑衍生物 |
| WO2003027114A1 (en) * | 2001-09-24 | 2003-04-03 | Bayer Pharmaceuticals Corporation | Preparation and use of 1,5,6,7-tetrahydropyrrolo[3,2-c]pyridine derivatives for treatment of obesity |
| GB0403780D0 (en) | 2004-02-20 | 2004-03-24 | Astrazeneca Ab | Therapeutic agents |
| EP1718617B1 (en) | 2004-02-20 | 2009-08-19 | AstraZeneca AB | 3-substituted 1,5-diphenylpyrazole derivatives useful as cb1 modulators |
| JP4177435B2 (ja) | 2004-04-03 | 2008-11-05 | アストラゼネカ アクチボラグ | 治療薬 |
| AR056560A1 (es) * | 2005-10-06 | 2007-10-10 | Astrazeneca Ab | Pirrolopiridinonas como moduladores cb1 |
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2006
- 2006-10-03 AR ARP060104347A patent/AR056560A1/es unknown
- 2006-10-04 UY UY29838A patent/UY29838A1/es unknown
- 2006-10-05 EP EP06794647A patent/EP1937679B1/en active Active
- 2006-10-05 DE DE602006008641T patent/DE602006008641D1/de active Active
- 2006-10-05 RU RU2008109185/04A patent/RU2415856C2/ru not_active IP Right Cessation
- 2006-10-05 BR BRPI0616653-9A patent/BRPI0616653A2/pt not_active IP Right Cessation
- 2006-10-05 ES ES06794647T patent/ES2329616T3/es active Active
- 2006-10-05 JP JP2008526558A patent/JP4277062B2/ja not_active Expired - Fee Related
- 2006-10-05 AU AU2006298530A patent/AU2006298530B2/en not_active Ceased
- 2006-10-05 CA CA002624495A patent/CA2624495A1/en not_active Abandoned
- 2006-10-05 WO PCT/GB2006/003695 patent/WO2007039740A2/en not_active Ceased
- 2006-10-05 US US11/915,643 patent/US7875626B2/en not_active Expired - Fee Related
- 2006-10-05 KR KR1020087010582A patent/KR20080058456A/ko not_active Withdrawn
- 2006-10-05 CN CNA2006800365273A patent/CN101277957A/zh active Pending
- 2006-10-05 TW TW095137255A patent/TW200730525A/zh unknown
- 2006-10-05 AT AT06794647T patent/ATE440099T1/de not_active IP Right Cessation
-
2007
- 2007-04-03 US US11/730,640 patent/US7576095B2/en not_active Expired - Fee Related
-
2008
- 2008-03-09 IL IL190025A patent/IL190025A0/en unknown
- 2008-03-28 NO NO20081523A patent/NO20081523L/no not_active Application Discontinuation
- 2008-04-03 ZA ZA200802946A patent/ZA200802946B/xx unknown
- 2008-04-30 EC EC2008008413A patent/ECSP088413A/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| BRPI0616653A2 (pt) | 2011-06-28 |
| US7875626B2 (en) | 2011-01-25 |
| ATE440099T1 (de) | 2009-09-15 |
| NO20081523L (no) | 2008-07-02 |
| TW200730525A (en) | 2007-08-16 |
| AU2006298530A1 (en) | 2007-04-12 |
| DE602006008641D1 (de) | 2009-10-01 |
| EP1937679B1 (en) | 2009-08-19 |
| US20080009513A1 (en) | 2008-01-10 |
| EP1937679A2 (en) | 2008-07-02 |
| ES2329616T3 (es) | 2009-11-27 |
| ZA200802946B (en) | 2009-03-25 |
| RU2008109185A (ru) | 2009-11-20 |
| US7576095B2 (en) | 2009-08-18 |
| HK1122808A1 (en) | 2009-05-29 |
| RU2415856C2 (ru) | 2011-04-10 |
| ECSP088413A (es) | 2008-05-30 |
| US20080312269A1 (en) | 2008-12-18 |
| CA2624495A1 (en) | 2007-04-12 |
| CN101277957A (zh) | 2008-10-01 |
| IL190025A0 (en) | 2008-08-07 |
| AU2006298530B2 (en) | 2009-10-29 |
| WO2007039740A2 (en) | 2007-04-12 |
| UY29838A1 (es) | 2007-05-31 |
| WO2007039740A3 (en) | 2007-05-31 |
| JP4277062B2 (ja) | 2009-06-10 |
| JP2009504722A (ja) | 2009-02-05 |
| KR20080058456A (ko) | 2008-06-25 |
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