CN1617718A - 用于治疗肥胖症的作为mch拮抗剂的n-芳基-n′-芳基环烷基脲衍生物 - Google Patents
用于治疗肥胖症的作为mch拮抗剂的n-芳基-n′-芳基环烷基脲衍生物 Download PDFInfo
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- CN1617718A CN1617718A CNA028277554A CN02827755A CN1617718A CN 1617718 A CN1617718 A CN 1617718A CN A028277554 A CNA028277554 A CN A028277554A CN 02827755 A CN02827755 A CN 02827755A CN 1617718 A CN1617718 A CN 1617718A
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- 0 N#CC(C1)=CC=CC1C1(C2)C2CC(*CCCC*C(CC2)C[C@@]2F)CC1 Chemical compound N#CC(C1)=CC=CC1C1(C2)C2CC(*CCCC*C(CC2)C[C@@]2F)CC1 0.000 description 5
- XFFNQTVMLMOELP-FZWJYZOSSA-N C=[I]c1cc(NC([O](CCCN(CC2)C[C@@H]2F)[C@H](CC2)CC(C3)C23c2cc(C#N)ccc2)=O)ccc1 Chemical compound C=[I]c1cc(NC([O](CCCN(CC2)C[C@@H]2F)[C@H](CC2)CC(C3)C23c2cc(C#N)ccc2)=O)ccc1 XFFNQTVMLMOELP-FZWJYZOSSA-N 0.000 description 1
- VISVBUTVDBCHMW-QLQAQYPDSA-N CC(C)CN1CCN(CCN([C@H](CC2)[C@@H]([C@H]3C)[C@]23c2cccc(C#N)c2)C(Nc(cc2C(F)(F)F)ccc2F)=O)CC1 Chemical compound CC(C)CN1CCN(CCN([C@H](CC2)[C@@H]([C@H]3C)[C@]23c2cccc(C#N)c2)C(Nc(cc2C(F)(F)F)ccc2F)=O)CC1 VISVBUTVDBCHMW-QLQAQYPDSA-N 0.000 description 1
- GIOHSGCUHBOFNI-NGQCZWSTSA-N CCCS(NC1CN(CCC[O]([C@H](CC2)CC(C3)[C@]23c2cc(C#N)ccc2)C(Nc(cc2Cl)ccc2F)=O)CC1)(=O)=O Chemical compound CCCS(NC1CN(CCC[O]([C@H](CC2)CC(C3)[C@]23c2cc(C#N)ccc2)C(Nc(cc2Cl)ccc2F)=O)CC1)(=O)=O GIOHSGCUHBOFNI-NGQCZWSTSA-N 0.000 description 1
- SWCLQEYWXXVPLK-DLKUSODMSA-N CCOC([N]1(CC1)C1CN(CCC[O]([C@H](CC2)CC(C3)[C@]23c2cccc(C#N)c2)C(Nc(cc2F)ccc2F)=O)CC1)=O Chemical compound CCOC([N]1(CC1)C1CN(CCC[O]([C@H](CC2)CC(C3)[C@]23c2cccc(C#N)c2)C(Nc(cc2F)ccc2F)=O)CC1)=O SWCLQEYWXXVPLK-DLKUSODMSA-N 0.000 description 1
- YMHWQPCPTVDMAF-XTDSVYKLSA-N CC[C@](C)(CC[C@H](C)[O](CCCN(CC1)CC1NC(C)=O)C(Nc(cc1F)ccc1F)=O)C(C=CC1)=CC1C#N Chemical compound CC[C@](C)(CC[C@H](C)[O](CCCN(CC1)CC1NC(C)=O)C(Nc(cc1F)ccc1F)=O)C(C=CC1)=CC1C#N YMHWQPCPTVDMAF-XTDSVYKLSA-N 0.000 description 1
- CJOUIPBXMVFOPJ-RWQQNZNLSA-N C[C@H]([C@@H]1[C@@H](CC2)N(CCCCN(C)C)C(Nc(cc3Cl)ccc3F)=O)[C@]12c1cccc(C#N)c1 Chemical compound C[C@H]([C@@H]1[C@@H](CC2)N(CCCCN(C)C)C(Nc(cc3Cl)ccc3F)=O)[C@]12c1cccc(C#N)c1 CJOUIPBXMVFOPJ-RWQQNZNLSA-N 0.000 description 1
- KNBNKWGVRNNKJH-BAWYACHWSA-N C[C@H]([C@@H]1[C@@H](CC2)N(CCCCN3CCN(C)CC3)C(Nc(cc3C(F)(F)F)ccc3F)=O)[C@]12c1cc(C#N)ccc1 Chemical compound C[C@H]([C@@H]1[C@@H](CC2)N(CCCCN3CCN(C)CC3)C(Nc(cc3C(F)(F)F)ccc3F)=O)[C@]12c1cc(C#N)ccc1 KNBNKWGVRNNKJH-BAWYACHWSA-N 0.000 description 1
- CDQFSAGUFOBQPC-UHFFFAOYSA-N N#Cc(cc1)ccc1C(CC1)=CCC1N(CCN1CCCC1)C(Nc1cc(F)cc(C(F)(F)F)c1)=O Chemical compound N#Cc(cc1)ccc1C(CC1)=CCC1N(CCN1CCCC1)C(Nc1cc(F)cc(C(F)(F)F)c1)=O CDQFSAGUFOBQPC-UHFFFAOYSA-N 0.000 description 1
- SCLHNMKPNODRRW-UHFFFAOYSA-N N#Cc1cc(C(CC2)=CCC2N(CCN2CCCC2)C(Nc2cc(F)cc(F)c2)=O)ccc1 Chemical compound N#Cc1cc(C(CC2)=CCC2N(CCN2CCCC2)C(Nc2cc(F)cc(F)c2)=O)ccc1 SCLHNMKPNODRRW-UHFFFAOYSA-N 0.000 description 1
- PADYOFAOFXVOGM-ONDZYYNLSA-N N#Cc1cc([C@](C2)(CC3)[C@H]2[C@@H]3N(CCCCN2CCCCC2)C(Nc(cc2C(F)(F)F)ccc2F)=O)ccc1 Chemical compound N#Cc1cc([C@](C2)(CC3)[C@H]2[C@@H]3N(CCCCN2CCCCC2)C(Nc(cc2C(F)(F)F)ccc2F)=O)ccc1 PADYOFAOFXVOGM-ONDZYYNLSA-N 0.000 description 1
- OIZHOXSNDPAUPE-QIGHUWCUSA-N N#Cc1cc([C@](C2)(CC3)[C@H]2[C@@H]3N(CCN2CCNCC2)C(Nc(cc2)cc(C(F)(F)F)c2F)=O)ccc1 Chemical compound N#Cc1cc([C@](C2)(CC3)[C@H]2[C@@H]3N(CCN2CCNCC2)C(Nc(cc2)cc(C(F)(F)F)c2F)=O)ccc1 OIZHOXSNDPAUPE-QIGHUWCUSA-N 0.000 description 1
- BJNIDUIQWUGXOW-DGWZTRNLSA-N N#Cc1ccc([C@](C2)(CC3)[C@H]2[C@@H]3N(CCN2CCCC2)C(Nc2cc(Cl)cc(Cl)c2)=O)cc1 Chemical compound N#Cc1ccc([C@](C2)(CC3)[C@H]2[C@@H]3N(CCN2CCCC2)C(Nc2cc(Cl)cc(Cl)c2)=O)cc1 BJNIDUIQWUGXOW-DGWZTRNLSA-N 0.000 description 1
- WVKGDXFNLLPPQP-WTIAFYNJSA-N N#Cc1cccc([C@H](CC2)CC[C@H]2N(CCN(CC2)C[C@@H]2O)C(Nc(cc2)cc(C(F)(F)F)c2F)=O)c1 Chemical compound N#Cc1cccc([C@H](CC2)CC[C@H]2N(CCN(CC2)C[C@@H]2O)C(Nc(cc2)cc(C(F)(F)F)c2F)=O)c1 WVKGDXFNLLPPQP-WTIAFYNJSA-N 0.000 description 1
- DJCLUEPPIAINHK-OROMBRFGSA-N N#Cc1cccc([C@](C2)(CC3)[C@H]2[C@@H]3N(CCCCN2CCOCC2)C(Nc(cc2C(F)(F)F)ccc2F)=O)c1 Chemical compound N#Cc1cccc([C@](C2)(CC3)[C@H]2[C@@H]3N(CCCCN2CCOCC2)C(Nc(cc2C(F)(F)F)ccc2F)=O)c1 DJCLUEPPIAINHK-OROMBRFGSA-N 0.000 description 1
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- C07D207/04—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 no double bonds between ring members or between ring members and non-ring members
- C07D207/08—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 no double bonds between ring members or between ring members and non-ring members with hydrocarbon radicals, substituted by hetero atoms, attached to ring carbon atoms
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- A61K31/40—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
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- C07D295/125—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
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- C07D405/06—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 carbon chain containing only aliphatic carbon atoms
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- C07C2601/14—The ring being saturated
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- C07C2602/14—All rings being cycloaliphatic
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- C07C2602/14—All rings being cycloaliphatic
- C07C2602/20—All rings being cycloaliphatic the ring system containing seven carbon atoms
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102875385A (zh) * | 2012-10-18 | 2013-01-16 | 浙江大学 | N,n-二异丙基乙胺的合成方法 |
| CN114269719A (zh) * | 2019-06-28 | 2022-04-01 | Rti国际 | 作为cb1变构调节剂的脲衍生物 |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
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| US7304065B2 (en) | 2003-10-01 | 2007-12-04 | The Procter & Gamble Company | Melanin concentrating hormone antagonists |
| WO2005034947A1 (en) * | 2003-10-02 | 2005-04-21 | Schering Corporation | Aminobenzimidazoles as selective melanin concentrating hormone receptor antagonists for the treatment of obesity and related disorders |
| DE102004003811A1 (de) * | 2004-01-25 | 2005-08-11 | Aventis Pharma Deutschland Gmbh | Substituierte N-Cyclohexylimidazolinone, Verfahren ihrer Herstellung und ihre Verwendung als Arzneimittel |
| EP2305352A1 (en) | 2004-04-02 | 2011-04-06 | Merck Sharp & Dohme Corp. | 5-alpha-reductase inhibitors for use in the treatment of men with metabolic and anthropometric disorders |
| EP1773822B1 (en) * | 2004-07-16 | 2009-06-17 | Shering Corporation | Heterocyclyls as selective melanin concentrating hormone receptor antagonists for the treatment of obesity and related disorders |
| US20070043100A1 (en) | 2005-08-16 | 2007-02-22 | Hagen Eric J | Novel polymorphs of azabicyclohexane |
| CA2583454A1 (en) * | 2004-10-12 | 2006-04-27 | Pharmacopeia Drug Discovery, Inc. | Bicyclic compounds as selective melanin concentrating hormone receptor antagonists for the treatment of obesity and related disorders |
| BRPI0518241A (pt) * | 2004-11-01 | 2008-04-22 | Amylin Pharmaceuticals Inc | métodos para tratar obesidade e doenças e distúrbios relacionados à obesidade |
| US8394765B2 (en) | 2004-11-01 | 2013-03-12 | Amylin Pharmaceuticals Llc | Methods of treating obesity with two different anti-obesity agents |
| AU2005305036B2 (en) * | 2004-11-01 | 2011-03-10 | Amylin Pharmaceuticals, Llc | Treatment of obesity and related disorders |
| US20090264650A1 (en) * | 2005-03-31 | 2009-10-22 | Nobuo Cho | Prophylactic/Therapeutic Agent for Diabetes |
| US7799943B2 (en) * | 2005-06-24 | 2010-09-21 | Rohm And Haas Company | Method for promoting Michael addition reactions |
| RU2008107336A (ru) | 2005-07-27 | 2009-09-10 | Дов Фармасьютикал, Инк. (Us) | Новые 1-арил-з-азабицикло{3.1.0.} гексаны: получение и применение для лечения психоневрологических расстройств |
| US20080045725A1 (en) | 2006-04-28 | 2008-02-21 | Murry Jerry A | Process For The Synthesis of (+) And (-)-1-(3,4-Dichlorophenyl)-3-Azabicyclo[3.1.0]Hexane |
| US20080269348A1 (en) * | 2006-11-07 | 2008-10-30 | Phil Skolnick | Novel Arylbicyclo[3.1.0]Hexylamines And Methods And Compositions For Their Preparation And Use |
| US8138377B2 (en) | 2006-11-07 | 2012-03-20 | Dov Pharmaceutical, Inc. | Arylbicyclo[3.1.0]hexylamines and methods and compositions for their preparation and use |
| US8030495B2 (en) * | 2007-05-23 | 2011-10-04 | Coleman Paul J | Cyclopropyl pyrrolidine orexin receptor antagonists |
| US9133159B2 (en) | 2007-06-06 | 2015-09-15 | Neurovance, Inc. | 1-heteroaryl-3-azabicyclo[3.1.0]hexanes, methods for their preparation and their use as medicaments |
| EP2036578A1 (en) * | 2007-09-13 | 2009-03-18 | Bayer Schering Pharma Aktiengesellschaft | Diagnostic agents for positron emission imaging using F-18 radio labeled amino-alcohols |
| US20140206740A1 (en) | 2011-07-30 | 2014-07-24 | Neurovance, Inc. | Use Of (1R,5S)-(+)-(Napthalen-2-yl)-3-Azabicyclo[3.1.0]Hexane In The Treatment Of Conditions Affected By Monoamine Neurotransmitters |
| WO2018026890A1 (en) | 2016-08-03 | 2018-02-08 | Cymabay Therapeutics | Oxymethylene aryl compounds for treating inflammatory gastrointestinal diseases or gastrointestinal conditions |
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| TW209868B (enExample) | 1991-04-04 | 1993-07-21 | Yoshitomi Pharmaceutical | |
| US5908830A (en) * | 1996-10-31 | 1999-06-01 | Merck & Co., Inc. | Combination therapy for the treatment of diabetes and obesity |
| CA2273102A1 (en) * | 1996-12-03 | 1998-06-11 | Banyu Pharmaceutical Co., Ltd. | Urea derivatives |
| CN1311773A (zh) * | 1998-06-08 | 2001-09-05 | 先灵公司 | 神经肽y5受体拮抗剂 |
| GB0010757D0 (en) * | 2000-05-05 | 2000-06-28 | Astrazeneca Ab | Chemical compounds |
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102875385A (zh) * | 2012-10-18 | 2013-01-16 | 浙江大学 | N,n-二异丙基乙胺的合成方法 |
| CN114269719A (zh) * | 2019-06-28 | 2022-04-01 | Rti国际 | 作为cb1变构调节剂的脲衍生物 |
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| HUP0500034A2 (hu) | 2005-04-28 |
| US20040122017A1 (en) | 2004-06-24 |
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| EP1453501A1 (en) | 2004-09-08 |
| AR037621A1 (es) | 2004-11-17 |
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| CA2468967A1 (en) | 2003-06-12 |
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| ATE404190T1 (de) | 2008-08-15 |
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| AU2002348269A1 (en) | 2003-06-17 |
| EP1453501B1 (en) | 2008-08-13 |
| JP2005511656A (ja) | 2005-04-28 |
| IL162311A0 (en) | 2005-11-20 |
| TW200302719A (en) | 2003-08-16 |
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