JP2009507034A5 - - Google Patents

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Publication number
JP2009507034A5
JP2009507034A5 JP2008529336A JP2008529336A JP2009507034A5 JP 2009507034 A5 JP2009507034 A5 JP 2009507034A5 JP 2008529336 A JP2008529336 A JP 2008529336A JP 2008529336 A JP2008529336 A JP 2008529336A JP 2009507034 A5 JP2009507034 A5 JP 2009507034A5
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JP
Japan
Prior art keywords
alkyl
group
optionally substituted
moiety
fluoro substituents
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JP2008529336A
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English (en)
Japanese (ja)
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JP2009507034A (ja
JP5155864B2 (ja
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Priority claimed from PCT/US2006/034335 external-priority patent/WO2007028083A2/en
Publication of JP2009507034A publication Critical patent/JP2009507034A/ja
Publication of JP2009507034A5 publication Critical patent/JP2009507034A5/ja
Application granted granted Critical
Publication of JP5155864B2 publication Critical patent/JP5155864B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

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JP2008529336A 2005-09-01 2006-09-01 5−HT2C受容体アゴニストとしての6−アリールアルキルアミノ−2,3,4,5−テトラヒドロ−1H−ベンゾ[d]アゼピン Expired - Fee Related JP5155864B2 (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
EP05380191 2005-09-01
EP05380191.6 2005-09-01
US73108105P 2005-10-28 2005-10-28
US60/731,081 2005-10-28
PCT/US2006/034335 WO2007028083A2 (en) 2005-09-01 2006-09-01 6-arylalkylamino- 2,3,4,5-tetrahydro-1h-benzo[d]azepines as 5-ht2c receptor agonists

Publications (3)

Publication Number Publication Date
JP2009507034A JP2009507034A (ja) 2009-02-19
JP2009507034A5 true JP2009507034A5 (https=) 2009-10-15
JP5155864B2 JP5155864B2 (ja) 2013-03-06

Family

ID=39892208

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2008529336A Expired - Fee Related JP5155864B2 (ja) 2005-09-01 2006-09-01 5−HT2C受容体アゴニストとしての6−アリールアルキルアミノ−2,3,4,5−テトラヒドロ−1H−ベンゾ[d]アゼピン

Country Status (13)

Country Link
US (2) US20080269196A1 (https=)
EP (1) EP1924561B1 (https=)
JP (1) JP5155864B2 (https=)
CN (1) CN101258131B (https=)
AU (1) AU2006287202B2 (https=)
BR (1) BRPI0615048A2 (https=)
CA (1) CA2619448C (https=)
DK (1) DK1924561T3 (https=)
ES (1) ES2397400T3 (https=)
PL (1) PL1924561T3 (https=)
PT (1) PT1924561E (https=)
SI (1) SI1924561T1 (https=)
WO (1) WO2007028083A2 (https=)

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WO2007028131A1 (en) * 2005-09-01 2007-03-08 Eli Lilly And Company 6-SUBSTITUTED 2,3,4,5-TETRAHYDRO-1H-BENZO[d]AZEPINES AS 5-HT2C RECEPTOR AGONISTS
JP5249031B2 (ja) * 2005-09-01 2013-07-31 イーライ リリー アンド カンパニー 5−HT2C受容体アゴニストとしての6−N結合型へテロ環置換された2,3,4,5−テトラヒドロ−1H−ベンゾ[d]アゼピン
EP2742936A1 (en) 2006-05-16 2014-06-18 Takeda Pharmaceutical Company Limited Fused heterocyclic compound and use thereof
WO2007140213A1 (en) 2006-05-26 2007-12-06 Forest Laboratories Holdings Limited Pyridoazepine derivatives
EP2789338A3 (en) 2007-11-15 2015-01-14 Takeda Pharmaceutical Company Limited Condensed pyridine derivate and use thereof
CA2722923C (en) 2008-04-29 2016-08-02 Boehringer Ingelheim International Gmbh Indazole compounds as ccr1 receptor antagonists
JP5411927B2 (ja) 2008-05-06 2014-02-12 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング Ccr1アンタゴニストとしてのピラゾール化合物
EP2346868B1 (en) 2008-09-26 2016-01-27 Boehringer Ingelheim International Gmbh Azaindazole compounds as ccr1 receptor antagonists
EP2491028B1 (en) 2009-10-21 2013-12-11 Boehringer Ingelheim International GmbH Indazole and pyrazolopyridine compounds as ccr1 receptor antagonists
EP2493875B1 (en) 2009-10-27 2014-08-06 Boehringer Ingelheim International GmbH Heterocyclic compounds as ccr1 receptor antagonists
CA2782384A1 (en) * 2009-12-08 2011-06-16 Boehringer Ingelheim International Gmbh Process for synthesis of intermediates useful for making substituted indazole and azaindazole compounds
WO2011137109A1 (en) 2010-04-30 2011-11-03 Boehringer Ingelheim International Gmbh Azaindazole amide compounds as ccr1 receptor antagonists
US20130267500A1 (en) 2010-09-01 2013-10-10 Arena Pharmaceuticals, Inc. 5-ht2c receptor agonists in the treatment of disorders ameliorated by reduction of norepinephrine level
EP2655371B1 (en) 2010-12-23 2015-02-25 Boehringer Ingelheim International GmbH Pyrazolopiperidine compounds as ccr1 receptor antagonists
US20140206667A1 (en) 2012-11-14 2014-07-24 Michela Gallagher Methods and compositions for treating schizophrenia
WO2015066344A1 (en) 2013-11-01 2015-05-07 Arena Pharmaceuticals, Inc. 5-ht2c receptor agonists and compositions and methods of use
EA201891526A3 (ru) * 2014-07-03 2019-05-31 Селджен Квонтисел Рисёрч, Инк. Ингибиторы лизин-специфической деметилазы-1
CN105622511B (zh) * 2014-11-03 2018-01-23 北京瑞都医药科技有限公司 一种减肥药物及其制备方法
CN109071440A (zh) * 2016-05-13 2018-12-21 日产化学株式会社 2-乙酰基吡啶化合物的制造方法
EP3733204A4 (en) 2017-12-27 2021-09-15 Takeda Pharmaceutical Company Limited THERAPEUTIC AGENT FOR URINARY INCONTINENCE OF STRESS AND FECAL INCONTINENCE
BR112022010021A2 (pt) * 2020-01-03 2022-08-16 Blue Oak Pharmaceuticals Inc Compostos e composições para tratamento de distúrbios do sistema nervoso central (snc)
CN114163426B (zh) * 2020-09-10 2024-03-19 上海爱博医药科技有限公司 苯并含氧杂环类化合物及其医药应用
GB202101734D0 (en) 2021-02-08 2021-03-24 Cerevance Inc Novel Compounds

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US5023252A (en) 1985-12-04 1991-06-11 Conrex Pharmaceutical Corporation Transdermal and trans-membrane delivery of drugs
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US4985352A (en) * 1988-02-29 1991-01-15 The Trustees Of Columbia University In The City Of New York DNA encoding serotonin 1C (5HT1c) receptor, isolated 5HT1c receptor, mammalian cells expressing same and uses thereof
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CN102329267A (zh) * 2004-02-25 2012-01-25 伊莱利利公司 作为5-HT2C受体激动剂的6-取代的2,3,4,5-四氢-1H-苯并[d]氮杂䓬
SI1838677T1 (sl) 2004-12-21 2010-01-29 Arena Pharm Inc Kristalne oblike (R)-8-kloro-1-metil-2,3,4,5-tetrahidro-1H-3-benzazepin hidroklorida
SG158168A1 (en) 2004-12-23 2010-01-29 Arena Pharm Inc 5ht2c receptor modulator compositions and methods of use
WO2007028131A1 (en) * 2005-09-01 2007-03-08 Eli Lilly And Company 6-SUBSTITUTED 2,3,4,5-TETRAHYDRO-1H-BENZO[d]AZEPINES AS 5-HT2C RECEPTOR AGONISTS

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