BRPI0511295A - 2-quinolil-oxazóis substituìdos úteis como inibidores de pde4 - Google Patents

2-quinolil-oxazóis substituìdos úteis como inibidores de pde4

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Publication number
BRPI0511295A
BRPI0511295A BRPI0511295-8A BRPI0511295A BRPI0511295A BR PI0511295 A BRPI0511295 A BR PI0511295A BR PI0511295 A BRPI0511295 A BR PI0511295A BR PI0511295 A BRPI0511295 A BR PI0511295A
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BR
Brazil
Prior art keywords
alkyl
cycloalkyl
pde4 inhibitors
quinolyl
hydroxyalkyl
Prior art date
Application number
BRPI0511295-8A
Other languages
English (en)
Inventor
Rongze Kuang
David Blythin
Neng-Yang Shih
Ho-Jane Shue
Xiao Chen
Jianhua Cao
Danlin Gu
Ying Huang
John N Schwerdt
Pauline C Ting
Shing-Chun Wong
Li Xiao
Original Assignee
Schering Corp
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Publication date
Application filed by Schering Corp filed Critical Schering Corp
Publication of BRPI0511295A publication Critical patent/BRPI0511295A/pt

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    • 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
    • A61K31/47—Quinolines; Isoquinolines
    • A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
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  • Chemical & Material Sciences (AREA)
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  • Health & Medical Sciences (AREA)
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  • Hospice & Palliative Care (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)

Abstract

2-QUINOLIL-OXAZóIS SUBSTITUìDOS úTEIS COMO INIBIDORES DE PDE4. A invenção refere-se a compostos da fórmula em que é uma heteroarila de 5 membros; X é S ou O; R¬ 1¬ é H, alquila, cicloalquila, cicloalquilalquila-, -CH~ 2~F, -CHF~ 2~, -CF~ 3~, -C(O)alquila ou -C(O)NR¬ 18¬R¬ 19¬; R¬ 3¬ e R¬ 4¬ H, alquila, hidroxialquila ou -C(O)Oalquila; R¬ 5 e R¬ 6¬ são H, alquila, hidroxialquila, alcoxialquila, mercaptoalquila, -CH~ 2~F, -CHF~ 2~, -CF~ 3~, -C(O)OH ou -C(O)Oalquila; R¬ 7¬ é H, alquila, alquenila, hidroxialquila, cicloalquila, alcoxialquila, aminoalquila, (R¬ 17¬-fenil)alquila ou -CH~ 2~-C(O)-O-alquila; e R¬ 8¬ compreende alquila, heteroarila, fenila ou cicloalquila, ou heterocicloalquila, todos opcionalmente substituídos, ou uma amida substituída por cicloalquila ou hetero-cicloalquila; ou R¬ 7¬ e R¬ 8¬ e o nitrogênio ao qual eles estão ligados conjuntamente formam um anel opcionalmente substituído; e as variáveis restantes são tais como definidas na especificação. Também são reivindicadas as composições farmacêuticas, o emprego dos compostos tais como inibidores de PDE4, e combinações com outros ativos.
BRPI0511295-8A 2004-05-18 2005-05-16 2-quinolil-oxazóis substituìdos úteis como inibidores de pde4 BRPI0511295A (pt)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US57226604P 2004-05-18 2004-05-18
PCT/US2005/017134 WO2005116009A1 (en) 2004-05-18 2005-05-16 Substituted 2-quinolyl-oxazoles useful as pde4 inhibitors

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BRPI0511295A true BRPI0511295A (pt) 2007-12-04

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US (1) US7511062B2 (pt)
EP (1) EP1758883B1 (pt)
JP (1) JP4584990B2 (pt)
KR (1) KR100907354B1 (pt)
CN (1) CN1984901B (pt)
AR (1) AR055192A1 (pt)
AT (1) ATE531705T1 (pt)
AU (1) AU2005247906B2 (pt)
BR (1) BRPI0511295A (pt)
CA (1) CA2565599C (pt)
EC (1) ECSP067013A (pt)
IL (1) IL179280A (pt)
MX (1) MXPA06013414A (pt)
NO (1) NO20065830L (pt)
NZ (1) NZ551017A (pt)
PE (1) PE20060241A1 (pt)
RU (1) RU2417993C9 (pt)
TW (1) TWI286475B (pt)
WO (1) WO2005116009A1 (pt)
ZA (1) ZA200609277B (pt)

Families Citing this family (67)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8682279B2 (en) 2004-05-07 2014-03-25 Interdigital Technology Corporation Supporting emergency calls on a wireless local area network
US8145182B2 (en) * 2004-05-07 2012-03-27 Interdigital Technology Corporation Supporting emergency calls on a wireless local area network
KR101122359B1 (ko) 2004-05-07 2012-03-23 인터디지탈 테크날러지 코포레이션 무선 근거리 통신망의 긴급 호 지원
EP2484382A1 (en) * 2005-03-30 2012-08-08 Schering Corporation Medicament comprising a phosphodiesterase IV inhibitor in an inhalable form
US7622496B2 (en) * 2005-12-23 2009-11-24 Zealand Pharma A/S Modified lysine-mimetic compounds
EP1997813B1 (en) * 2006-03-10 2010-05-05 Nissan Chemical Industries, Ltd. Substituted isoxazoline compound and pest control agent
EA200802058A1 (ru) * 2006-05-09 2009-06-30 Пфайзер Продактс Инк. Производные циклоалкиламинокислот и их фармацевтические композиции
JP5352452B2 (ja) * 2006-06-06 2013-11-27 メディシノバ, インコーポレイテッド 置換ピラゾロ[1,5−a]ピリジン化合物およびその使用方法
US8138205B2 (en) * 2006-07-07 2012-03-20 Kalypsys, Inc. Heteroarylalkoxy-substituted quinolone inhibitors of PDE4
US8080563B2 (en) * 2006-07-07 2011-12-20 Kalypsys Bicyclic heteroaryl inhibitors of PDE4
WO2008008327A2 (en) 2006-07-11 2008-01-17 Schering Corporation Xinafoate salt of a substituted 5-oxazol-2-yl-quinoline compound
ITMI20061581A1 (it) * 2006-08-04 2008-02-05 Univ Bari Ligandi del recettore beta-3 adrenergico e loro uso in terapia
CN101522671A (zh) * 2006-08-14 2009-09-02 先灵公司 5-(1(s)-氨基-2-羟基乙基)-n-[(2,4-二氟苯基)-甲基]-2-[8-甲氧基-2-(三氟甲基)-5-喹啉]-4-唑甲酰胺的顺丁烯二酸盐、甲苯磺酸盐、反丁烯二酸盐和草酸盐盐类,及其制备方法
AU2007284688A1 (en) * 2006-08-14 2008-02-21 Schering Corporation Process and intermediates for the synthesis of 2-(Quinolin-5-yl)-4,5 Disubstituted-Azole derivatives
AR062841A1 (es) * 2006-09-15 2008-12-10 Schering Corp Tratamiento del dolor, diabetes, y trastornos del metabolismo de los lipidos
EP2061796A2 (en) 2006-09-15 2009-05-27 Schering Corporation Azetidine and azetidinone derivatives useful in treating pain and disorders of lipid metabolism
JP2010503675A (ja) 2006-09-15 2010-02-04 シェーリング コーポレイション 疼痛、糖尿病および脂質代謝の障害の治療に有用なスピロ縮合アゼチジン誘導体
US20100210633A1 (en) * 2006-10-12 2010-08-19 Epix Delaware, Inc. Carboxamide compounds and their use
JP2008260691A (ja) * 2007-04-10 2008-10-30 Bayer Cropscience Ag 殺虫性アリールイソオキサゾリン誘導体
JP4986927B2 (ja) * 2007-05-14 2012-07-25 大塚製薬株式会社 医薬
US20110171195A1 (en) * 2007-06-15 2011-07-14 Duke University Methods and compositions for treating urinary tract infections using agents that mimic or elevate cyclic amp
US20100324295A1 (en) * 2007-07-10 2010-12-23 Schering Corporation Process for the production of substituted 5-quinolyl-oxazoles and pharmaceutically acceptable salts thereof
EP2176257A2 (en) * 2007-07-10 2010-04-21 Schering Corporation Hydrogen chloride salt of a substituted 5-oxazol-2-yl-quinoline compound and a process for the production thereof
GB2451629A (en) * 2007-08-06 2009-02-11 Univ Sheffield 1-(Azolylcarbonyl)-2-(hydroxymethyl)pyrrolidine derivatives for use as catalysts for asymmetric reduction of imines & reductive amination of ketones
AU2008335135A1 (en) 2007-12-11 2009-06-18 Cytopathfinder, Inc. Carboxamide compounds and their use as chemokine receptor agonists
EP2098526B1 (en) * 2008-02-22 2014-01-15 Neurotune AG Nitrogen-containing bicyclic compounds active on chronic pain conditions
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
AR074318A1 (es) * 2008-11-14 2011-01-05 Nycomed Gmbh Derivados heterociclicos de pirazolona, composiciones farmaceuticas que los contienen y uso de los mismos para el tratamiento de enfermedades de las vias respiratorias.
JP5476895B2 (ja) 2008-12-17 2014-04-23 セントラル硝子株式会社 ヒドロキシル基置換生成物の製造方法
JP5683489B2 (ja) * 2009-01-12 2015-03-11 アレイ バイオファーマ、インコーポレイテッド ピペリジン含有化合物およびその用途
US8796297B2 (en) 2009-06-30 2014-08-05 Abbvie Inc. 4-substituted-2-amino-pyrimidine derivatives
WO2011029802A1 (en) * 2009-09-08 2011-03-17 F. Hoffmann-La Roche Ag 4-substituted pyridin-3-yl-carboxamide compounds and methods of use
KR101483215B1 (ko) 2010-01-29 2015-01-16 한미약품 주식회사 단백질 키나아제 저해활성을 갖는 비시클릭 헤테로아릴 유도체
CN103221404B (zh) 2010-05-13 2015-12-16 安姆根有限公司 可用作pde10抑制剂的不饱和氮杂环化合物
JP5709101B2 (ja) * 2010-09-01 2015-04-30 東レ・ファインケミカル株式会社 ヒドロキシプロリン誘導体の製造法
GB2497476B (en) * 2010-09-06 2018-01-10 Guangzhou Inst Biomed & Health Amide Compounds
WO2012072512A1 (en) 2010-11-29 2012-06-07 Glaxo Group Limited N-cyclobutyl-imidazopyridine or -pyrazolopyridine carboxamides as trpv1 antagonists
CN102408433B (zh) * 2011-10-20 2014-04-09 天津药物研究院 含嘧啶的肟类化合物、其制备方法和用途
US8530461B2 (en) * 2011-12-29 2013-09-10 Boehringer Ingelheim International Gmbh Azetidine derivatives
RU2014146993A (ru) 2012-04-24 2016-06-10 Чугаи Сейяку Кабусики Кайся Производное хиназолиндиона
MX2014012991A (es) * 2012-04-24 2015-08-14 Chugai Pharmaceutical Co Ltd Derivado de benzamida.
US8865723B2 (en) 2012-10-25 2014-10-21 Tetra Discovery Partners Llc Selective PDE4 B inhibition and improvement in cognition in subjects with brain injury
MX364895B (es) * 2013-03-13 2019-05-10 Forma Therapeutics Inc Nuevos compuestos y composiciones para la inhibicion de fasn.
US9938291B2 (en) 2013-03-14 2018-04-10 The Trustess Of Columbia University In The City Of New York N-alkyl-2-phenoxyethanamines, their preparation and use
EP2968303B1 (en) 2013-03-14 2018-07-04 The Trustees of Columbia University in the City of New York Octahydrocyclopentapyrroles, their preparation and use
US10273243B2 (en) 2013-03-14 2019-04-30 The Trustees Of Columbia University In The City Of New York 4-phenylpiperidines, their preparation and use
US9944644B2 (en) 2013-03-14 2018-04-17 The Trustees Of Columbia University In The City Of New York Octahydropyrrolopyrroles their preparation and use
CA2927830A1 (en) 2013-10-23 2015-04-30 Chugai Seiyaku Kabushiki Kaisha Quinazolinone and isoquinolinone derivative
CN105085428B (zh) * 2014-04-25 2019-03-22 广东东阳光药业有限公司 芳杂环类衍生物及其在药物上的应用
CN111393434B (zh) 2014-04-30 2022-11-04 哥伦比亚大学董事会 取代的4-苯基哌啶及其制备和用途
GB201415569D0 (en) 2014-09-03 2014-10-15 C4X Discovery Ltd Therapeutic Compounds
JP2018016544A (ja) * 2014-12-03 2018-02-01 持田製薬株式会社 新規ジアザビシクロ[2.2.2]オクタン誘導体
CN104829492A (zh) * 2015-05-06 2015-08-12 河北工业大学 一种反式N-Boc-1,3-环丁二胺的制备方法
CN106279138B (zh) * 2015-12-29 2019-03-01 广东东阳光药业有限公司 芳杂环类衍生物及其在药物中的应用
GB201601703D0 (en) 2016-01-29 2016-03-16 C4X Discovery Ltd Therapeutic compounds
CN111727042A (zh) 2017-12-06 2020-09-29 仁新医药私人有限公司 微管蛋白抑制剂
JP7184383B2 (ja) * 2018-02-01 2022-12-06 ザ・ユニバーシティ・オブ・シドニー 抗癌性化合物
KR102682705B1 (ko) * 2018-07-04 2024-07-05 고려대학교 세종산학협력단 옥사졸로퀴놀리논 유도체를 유효성분으로 포함하는 우울증 및 스트레스 관련 질환의 예방 또는 치료용 약학 조성물
DK3808747T3 (da) * 2018-09-13 2025-02-03 Kissei Pharmaceutical Imidazopyridinon-forbindelse
TWI767148B (zh) 2018-10-10 2022-06-11 美商弗瑪治療公司 抑制脂肪酸合成酶(fasn)
CN113382633A (zh) 2018-10-29 2021-09-10 福马治疗股份有限公司 (4-(2-氟-4-(1-甲基-1H-苯并[d]咪唑-5-基)苯甲酰基)哌嗪-1-基)(1-羟基环丙基)甲酮的固体形式
CN112079791A (zh) * 2020-08-21 2020-12-15 宁夏农林科学院农业资源与环境研究所(宁夏土壤与植物营养重点实验室) 单环β-内酰胺类抗生素侧链酸及其酯、其制备方法和应用
CN116963773B (zh) 2021-01-21 2026-05-08 浙江养生堂天然药物研究所有限公司 治疗肿瘤的组合物及方法
EP4469460A1 (en) * 2022-01-28 2024-12-04 Bioage Labs, Inc. N-oxide inhibitors of nlrp3 inflammasome
TWI907890B (zh) * 2022-12-14 2025-12-11 國立成功大學 化合物及其合成方法與應用
WO2025207644A1 (en) 2024-03-26 2025-10-02 BioAge Labs, Inc. Inhibitors of nlrp3 inflammasome
CN121627594B (zh) * 2026-02-02 2026-05-08 五邑大学 一种双靶点抑制剂及其制备方法和应用

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000510866A (ja) 1996-05-20 2000-08-22 ダーウィン・ディスカバリー・リミテッド Tnfとpde―ivのインヒビターとしてのキノリンスルホンアミド
NZ332341A (en) 1996-05-20 2000-05-26 Darwin Discovery Ltd Quinoline carboxamides as TNF inhibitors and as PDE-IV inhibitors
DE69723863T2 (de) 1996-11-06 2004-04-15 Darwin Discovery Ltd., Slough Chinoline und deren therapeutische verwendung
US6069151A (en) * 1996-11-06 2000-05-30 Darwin Discovery, Ltd. Quinolines and their therapeutic use
EP1042295B1 (en) * 1997-12-22 2005-09-07 Pharmacia & Upjohn Company LLC 4-hydroxyquinoline-3-carboxamides and hydrazides as antiviral agents
ATE247652T1 (de) * 1999-03-29 2003-09-15 Neurogen Corp 4-substituierte chinolinderivate als nk-3 und/oder gaba(a) rezeptor liganden
US6569885B1 (en) * 1999-12-23 2003-05-27 Icos Corporation Cyclic AMP-specific phosphodiesterase inhibitors
GB0003254D0 (en) * 2000-02-11 2000-04-05 Darwin Discovery Ltd Heterocyclic compounds and their therapeutic use
JP4790969B2 (ja) 2000-08-11 2011-10-12 日本ケミファ株式会社 ペルオキシソーム増殖剤応答性受容体δの活性化剤
JP4157381B2 (ja) 2001-03-23 2008-10-01 日本ケミファ株式会社 ペルオキシソーム増殖剤応答性受容体の活性化剤
DE10227269A1 (de) 2002-06-19 2004-01-08 Merck Patent Gmbh Thiazolderivate
WO2008008327A2 (en) * 2006-07-11 2008-01-17 Schering Corporation Xinafoate salt of a substituted 5-oxazol-2-yl-quinoline compound

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