WO2008123469A1 - 6員環アミド化合物およびその用途 - Google Patents

6員環アミド化合物およびその用途 Download PDF

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Publication number
WO2008123469A1
WO2008123469A1 PCT/JP2008/056237 JP2008056237W WO2008123469A1 WO 2008123469 A1 WO2008123469 A1 WO 2008123469A1 JP 2008056237 W JP2008056237 W JP 2008056237W WO 2008123469 A1 WO2008123469 A1 WO 2008123469A1
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amide compound
membered
membered amide
compound
disclosed
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PCT/JP2008/056237
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English (en)
French (fr)
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Tetsuya Iida
Ikuo Mitani
Yuichi Nakagawa
Masahiro Tanaka
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Japan Tobacco Inc.
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Publication of WO2008123469A1 publication Critical patent/WO2008123469A1/ja

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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings 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
    • C07D211/36Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings 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 hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D211/56Nitrogen atoms
    • C07D211/58Nitrogen atoms attached in position 4
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/08Antiseborrheics
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
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    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/06Antihyperlipidemics
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
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    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C237/00Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
    • C07C237/28Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton
    • C07C237/40Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton having the nitrogen atom of the carboxamide group bound to a carbon atom of a six-membered aromatic ring
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    • C07D213/24Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
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    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/78Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
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    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
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    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D277/32Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D277/38Nitrogen atoms
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    • C07D277/20Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
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    • C07D277/62Benzothiazoles
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    • C07D513/04Ortho-condensed systems

Abstract

 優れたSCD1活性阻害作用を有する化合物を提供すること。下記一般式[B-0’]で表される化合物又はその医薬上許容される塩、或いはその溶媒和物: [式中、各記号は明細書中で定義した通りである。]。
PCT/JP2008/056237 2007-03-30 2008-03-28 6員環アミド化合物およびその用途 WO2008123469A1 (ja)

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JP2007-095639 2007-03-30
JP2007095639 2007-03-30
US92581607P 2007-04-23 2007-04-23
US60/925,816 2007-04-23

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WO2008123469A1 true WO2008123469A1 (ja) 2008-10-16

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Cited By (23)

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EP2202228A1 (en) * 2007-10-15 2010-06-30 Takeda Pharmaceutical Company Limited Amide compounds and use of the same
JP2011051931A (ja) * 2009-09-01 2011-03-17 Sagami Chemical Research Institute 2−アシルアミノチアゾール誘導体及びその製造方法
WO2013056148A2 (en) 2011-10-15 2013-04-18 Genentech, Inc. Methods of using scd1 antagonists
WO2013061297A1 (en) * 2011-10-28 2013-05-02 Pfizer Limited Pyridazine Derivatives Useful in Therapy
JP2013544806A (ja) * 2010-11-01 2013-12-19 ロマーク ラボラトリース,エル.シー. アルキルスルフィニル置換チアゾリド化合物
JP2014520886A (ja) * 2011-07-18 2014-08-25 メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング ベンズアミド類
JP2016164177A (ja) * 2010-08-23 2016-09-08 シントリックス・バイオシステムズ・インコーポレイテッドSyntrix Biosystems, Inc. Cxcr2モジュレーターとしてのアミノピリジンカルボキサミドおよびアミノピリミジンカルボキサミド
US9707248B2 (en) 2013-08-02 2017-07-18 Syntrix Biosystems Inc. Use of thiopyrimidinecarboxamide for treating cancer
WO2018028517A1 (en) * 2016-08-12 2018-02-15 Eli Lilly And Company Amino pyrimidine ssao inhibitors
US10046002B2 (en) 2013-08-02 2018-08-14 Syntrix Biosystems Inc. Method for treating cancer using chemokine antagonists
JP2018522983A (ja) * 2015-07-20 2018-08-16 イリドス リミテッド 着色剤化合物及びこれを含む着色剤材料
CN109354580A (zh) * 2018-11-21 2019-02-19 山东罗欣药业集团股份有限公司 一种盐酸多奈哌齐的制备方法
USRE47267E1 (en) 2009-02-17 2019-03-05 Syntrix Biosystems, Inc. Pyridinecarboxamides as CXCR2 modulators
US10278970B2 (en) 2017-02-14 2019-05-07 Eli Lilly And Company Amino pyrimidine compounds useful as SSAO inhibitors
CN103450112B (zh) * 2013-08-07 2019-09-13 华东理工大学 一种n-桥连接的含氮五元杂环化合物及其制备与用途
US10561676B2 (en) 2013-08-02 2020-02-18 Syntrix Biosystems Inc. Method for treating cancer using dual antagonists of CXCR1 and CXCR2
US10660909B2 (en) 2016-11-17 2020-05-26 Syntrix Biosystems Inc. Method for treating cancer using chemokine antagonists
JP2020524178A (ja) * 2017-05-24 2020-08-13 ヨハン ヴォルフガング ゲーテ−ウニヴェルズィテート フランクフルト アム マイン ファルネソイドx受容体および可溶性エポキシドヒドロラーゼの二重調節剤
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US11820754B2 (en) 2020-08-25 2023-11-21 Eli Lilly And Company Polymorphs of an SSAO inhibitor
US11873298B2 (en) 2017-10-24 2024-01-16 Janssen Pharmaceutica Nv Compounds and uses thereof
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Cited By (50)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2202228A1 (en) * 2007-10-15 2010-06-30 Takeda Pharmaceutical Company Limited Amide compounds and use of the same
EP2202228A4 (en) * 2007-10-15 2011-06-29 Takeda Pharmaceutical AMIDE COMPOUNDS AND THEIR USE
US8329691B2 (en) 2007-10-15 2012-12-11 Takeda Pharmaceutical Company Limited Amide compounds and use of the same
USRE47267E1 (en) 2009-02-17 2019-03-05 Syntrix Biosystems, Inc. Pyridinecarboxamides as CXCR2 modulators
USRE47415E1 (en) 2009-02-17 2019-06-04 Syntrix Biosystems, Inc. Pyrimidinecarboxamides as CXCR2 modulators
JP2011051931A (ja) * 2009-09-01 2011-03-17 Sagami Chemical Research Institute 2−アシルアミノチアゾール誘導体及びその製造方法
JP2019069946A (ja) * 2010-08-23 2019-05-09 シントリックス・バイオシステムズ・インコーポレイテッドSyntrix Biosystems, Inc. Cxcr2モジュレーターとしてのアミノピリジンカルボキサミドおよびアミノピリミジンカルボキサミド
USRE47740E1 (en) 2010-08-23 2019-11-26 Syntrix Biosystems Inc. Aminopyridinecarboxamides as CXCR2 modulators
JP2016164177A (ja) * 2010-08-23 2016-09-08 シントリックス・バイオシステムズ・インコーポレイテッドSyntrix Biosystems, Inc. Cxcr2モジュレーターとしてのアミノピリジンカルボキサミドおよびアミノピリミジンカルボキサミド
USRE48547E1 (en) 2010-08-23 2021-05-11 Syntrix Biosystems Inc. Aminopyrimidinecarboxamides as CXCR2 modulators
JP2013544806A (ja) * 2010-11-01 2013-12-19 ロマーク ラボラトリース,エル.シー. アルキルスルフィニル置換チアゾリド化合物
JP2014520886A (ja) * 2011-07-18 2014-08-25 メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング ベンズアミド類
US9938262B2 (en) 2011-07-18 2018-04-10 Merck Patent Gmbh Benzamides
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