OA13365A - Substituted quinoline compounds. - Google Patents

Substituted quinoline compounds. Download PDF

Info

Publication number
OA13365A
OA13365A OA1200600247A OA1200600247A OA13365A OA 13365 A OA13365 A OA 13365A OA 1200600247 A OA1200600247 A OA 1200600247A OA 1200600247 A OA1200600247 A OA 1200600247A OA 13365 A OA13365 A OA 13365A
Authority
OA
OAPI
Prior art keywords
alkyl
group
phenyl
halo
compound
Prior art date
Application number
OA1200600247A
Other languages
English (en)
Inventor
Peter Bertinato
Michel Andre Couturier
Marcus Douglas Ewing
Ernest Seiichi Hamanaka
Ralph Pelton Robinson Jr
Derek Lawrence Tickner
Original Assignee
Pfizer Prod Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Pfizer Prod Inc filed Critical Pfizer Prod Inc
Publication of OA13365A publication Critical patent/OA13365A/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic 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
    • 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
    • C07D215/48Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/4709Non-condensed quinolines and containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/04Anorexiants; Antiobesity agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/06Antihyperlipidemics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Diabetes (AREA)
  • Obesity (AREA)
  • Hematology (AREA)
  • Urology & Nephrology (AREA)
  • Endocrinology (AREA)
  • Child & Adolescent Psychology (AREA)
  • Emergency Medicine (AREA)
  • Vascular Medicine (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Quinoline Compounds (AREA)
OA1200600247A 2004-02-04 2005-01-24 Substituted quinoline compounds. OA13365A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US54167804P 2004-02-04 2004-02-04
US63376304P 2004-12-06 2004-12-06

Publications (1)

Publication Number Publication Date
OA13365A true OA13365A (en) 2007-04-13

Family

ID=34890449

Family Applications (1)

Application Number Title Priority Date Filing Date
OA1200600247A OA13365A (en) 2004-02-04 2005-01-24 Substituted quinoline compounds.

Country Status (25)

Country Link
US (3) US7468378B2 (fr)
EP (1) EP1716137A1 (fr)
JP (1) JP2007520543A (fr)
KR (1) KR100799802B1 (fr)
AP (1) AP2006003685A0 (fr)
AR (1) AR047529A1 (fr)
AU (1) AU2005214159A1 (fr)
BR (1) BRPI0507462A (fr)
CA (1) CA2555133A1 (fr)
CO (1) CO5700721A2 (fr)
CR (1) CR8544A (fr)
EA (1) EA010369B1 (fr)
EC (1) ECSP066717A (fr)
GE (1) GEP20084360B (fr)
IL (2) IL176715A0 (fr)
MA (1) MA28347A1 (fr)
NL (1) NL1028192C2 (fr)
NO (1) NO20063928L (fr)
OA (1) OA13365A (fr)
PA (1) PA8623001A1 (fr)
PE (1) PE20050773A1 (fr)
SV (1) SV2007002007A (fr)
TW (2) TWI306454B (fr)
UY (1) UY28734A1 (fr)
WO (1) WO2005080373A1 (fr)

Families Citing this family (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105820160B (zh) 2003-11-05 2019-02-12 萨可德生物科学公司 细胞粘着调节剂
AP2006003685A0 (en) * 2004-02-04 2006-08-31 Pfizer Prod Inc Substituted quinoline compounds
US7262318B2 (en) * 2004-03-10 2007-08-28 Pfizer, Inc. Substituted heteroaryl- and phenylsulfamoyl compounds
EP1740553A1 (fr) * 2004-04-14 2007-01-10 AstraZeneca AB Derives d'aryle glycinamide et utilisation en tant qu'antagonistes de nk1 et en tant qu'inhibiteurs du recaptage de serotonine
PA8660701A1 (es) 2005-02-04 2006-09-22 Pfizer Prod Inc Agonistas de pyy y sus usos
WO2006113910A2 (fr) 2005-04-19 2006-10-26 Surface Logix, Inc. Inhibiteurs des secretions microsomales des apo-b et des proteines de transfert des triglycerides
WO2008050199A2 (fr) * 2006-10-23 2008-05-02 Pfizer Japan Inc. Composés de phénylméthyl bicyclocarboxyamide substitués
KR20090064478A (ko) 2006-11-13 2009-06-18 화이자 프로덕츠 인크. 디아릴, 디피리디닐 및 아릴-피리디닐 유도체, 및 이들의 용도
EP2115368A1 (fr) * 2007-02-02 2009-11-11 Steve D. Shivvers Dispositif de séchage à haut rendement équipé de zones de chauffage et de séchage à plusieurs étages
WO2008100423A1 (fr) * 2007-02-09 2008-08-21 Sirtris Pharmaceuticals, Inc. Inhibiteurs de protéines microsomiques de transport des triglycérides de l'intestin
WO2009014674A1 (fr) * 2007-07-23 2009-01-29 Sirtris Pharmaceuticals, Inc. Hétérocyclylamides comme inhibiteurs de la protéine de transport de triglycérides microsomal de l'intestin
EP2214481B1 (fr) 2007-10-15 2019-05-01 United Animal Health, Inc. Procédé permettant d'accroître la performance d'une progéniture
EP3797775A1 (fr) 2007-10-19 2021-03-31 Novartis AG Compositions et procédés pour le traitement de la rétinopathie diabétique
WO2010018547A1 (fr) * 2008-08-13 2010-02-18 Pfizer Inc. Composés aminoquinoline
MX2013015274A (es) 2011-06-24 2014-03-31 Amgen Inc Anatagonista trpm8 y su uso en tratamientos.
JP2014517074A (ja) 2011-06-24 2014-07-17 アムジエン・インコーポレーテツド Trpm8アンタゴニストおよび治療におけるそれらの使用
CN103958502B (zh) * 2011-08-04 2016-02-10 阵列生物制药公司 作为丝氨酸/苏氨酸激酶抑制剂的喹唑啉化合物
US8952009B2 (en) 2012-08-06 2015-02-10 Amgen Inc. Chroman derivatives as TRPM8 inhibitors
EP3107540A4 (fr) * 2014-02-17 2017-08-30 Hetero Research Foundation Polymorphes de lomitapide et ses sels
EP3798214B1 (fr) 2014-10-06 2022-09-14 Vertex Pharmaceuticals Incorporated Modulateurs de régulateur de conductance transmembranaire de la fibrose kystique
US10138206B2 (en) 2014-10-09 2018-11-27 Glenmark Pharmaceuticals Limited Amorphous form of lomitapide mesylate
CA3019380A1 (fr) 2016-03-31 2017-10-05 Vertex Pharmaceuticals Incorporated Modulateurs du regulateur de la conductance transmembranaire de la fibrose kystique
ES2900263T3 (es) 2016-09-30 2022-03-16 Vertex Pharma Modulador de regulador de conductancia transmembrana de fibrosis quística, composiciones farmacéuticas, métodos de tratamiento y proceso de fabricación del modulador
JOP20190125B1 (ar) 2016-12-09 2022-03-14 Vertex Pharma مُعدِّل‏ لمنظم موصلية التليف الكيسي عبر الغشاء، وتركيبات صيدلانية، وطرق للعلاج، وعملية لتصنيع المُعدِّل
CA3066084A1 (fr) 2017-06-08 2018-12-13 Vertex Pharmaceuticals Incorporated Methodes de traitement de la fibrose kystique
EP3654969A1 (fr) 2017-07-17 2020-05-27 Vertex Pharmaceuticals Incorporated Méthodes de traitement de la fibrose kystique
TWI799435B (zh) 2017-08-02 2023-04-21 美商維泰克斯製藥公司 製備化合物之製程
CA3078893A1 (fr) 2017-10-19 2019-04-25 Vertex Pharmaceuticals Incorporated Formes cristallines et compositions de modulateurs de cftr
EP3720849A2 (fr) 2017-12-08 2020-10-14 Vertex Pharmaceuticals Incorporated Procédés pour préparer des modulateurs du régulateur de la conductance transmembranaire de la mucoviscidose
TWI810243B (zh) 2018-02-05 2023-08-01 美商維泰克斯製藥公司 用於治療囊腫纖化症之醫藥組合物
EP3774825A1 (fr) 2018-04-13 2021-02-17 Vertex Pharmaceuticals Incorporated Modulateurs du régulateur de la conductance transmembranaire de la fibrose kystique, compositions pharmaceutiques, procédés de traitement et procédé de fabrication du modulateur

Family Cites Families (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2819039A1 (de) 1978-04-29 1979-11-08 Bayer Ag Leimungsmittel fuer papier
AU558909B2 (en) 1981-03-11 1987-02-12 Wellcome Foundation Limited, The Biphenyl compounds
KR0182801B1 (ko) 1991-04-16 1999-05-01 아만 히데아키 고체 분산체의 제조방법
US5595872A (en) 1992-03-06 1997-01-21 Bristol-Myers Squibb Company Nucleic acids encoding microsomal trigyceride transfer protein
CA2091102C (fr) 1992-03-06 2009-05-26 John R. Ii Wetterau Proteine de transfert de triglycerides microsomaux
US5739135A (en) 1993-09-03 1998-04-14 Bristol-Myers Squibb Company Inhibitors of microsomal triglyceride transfer protein and method
CZ291476B6 (cs) 1994-05-27 2003-03-12 Smithkline Beecham S. P. A. N-(alfa-Ethylbenzyl)-3-hydroxy-2-fenylchinolin-4-karboxamid, farmaceutický prostředek s jeho obsahem a použití
DE19504832A1 (de) 1995-02-14 1996-08-22 Basf Ag Feste Wirkstoff-Zubereitungen
DE19519245C2 (de) * 1995-04-14 2003-04-30 Boehringer Ingelheim Kg Neue Arylglycinamidderivate, Verfahren zu ihrer Herstellung und diese Verbindungen enthaltende pharmazeutische Zusammensetzungen
DK0832069T3 (da) 1995-06-07 2003-04-22 Pfizer Biphenyl-2-carboxylsyre-tetrahydroisoquinolin-6-ylamidderivater, deres fremstilling og deres anvendelse som inhibitorer af sekretion af mikrosomalt triglyceridoverførselsprotein og/eller apolipoprotein B (Apo B)
WO1996040640A1 (fr) 1995-06-07 1996-12-19 Pfizer Inc. DERIVES DE BIPHENYL-2-ACIDE CARBOXYLIQUE-TETRAHYDRO-ISOQUINOLEINE-6-YL AMIDES, PREPARATION DE CES AMIDES ET UTILISATION EN TANT QU'INHIBITEURS DE LA PROTEINE DE TRANSFERT DE TRIGLYCERIDE MICROSOMAL ET/OU DE LA SECRETION D'APOLIPOPROTEINES B (Apo B)
US5827875A (en) 1996-05-10 1998-10-27 Bristol-Myers Squibb Company Inhibitors of microsomal triglyceride transfer protein and method
SK283162B6 (sk) * 1996-05-20 2003-03-04 Darwin Discovery Limited Karboxamid chinolínu ako inhibítor faktora nekrotizujúceho nádor, inhibítor fosfodiesterázy-IV a farmaceutický prostriedok s jeho obsahom
JP2000515501A (ja) 1996-07-01 2000-11-21 イーライ・リリー・アンド・カンパニー 低血糖化および低脂血化用化合物群
KR100217618B1 (ko) * 1996-12-12 1999-09-01 정몽규 와셔액 분사위치 조절 장치
WO1998027979A1 (fr) 1996-12-20 1998-07-02 Bristol-Myers Squibb Company Inhibiteurs heterocycliques de la proteine de transfert des triglycerides microsomiques et methode associee
US6066653A (en) 1997-01-17 2000-05-23 Bristol-Myers Squibb Co. Method of treating acid lipase deficiency diseases with an MTP inhibitor and cholesterol lowering drugs
US5968950A (en) 1997-06-23 1999-10-19 Pfizer Inc Apo B-secretion/MTP inhibitor hydrochloride salt
ES2287971T3 (es) 1997-08-11 2007-12-16 Pfizer Products Inc. Dispersiones farmaceuticas solidas con biodisponibilidad incrementada.
AP1201A (en) 1997-09-17 2003-09-01 Smithkline Beecham Corp Method for the synthesis of quinoline derivatives.
CA2309882A1 (fr) * 1997-12-22 1999-07-01 Pharmacia & Upjohn Company 4-hydroxyquinoline-3-carboxamides et hydrazides utilises comme agents antiviraux
CO5090829A1 (es) 1998-07-21 2001-10-30 Novartis Ag Compuestos organicos de la formula i, utiles como inhibido res de la proteina de transferencia de triglicerido microso mal y de la secrecion de la apolipoproteina b.
CA2325358C (fr) 1999-11-10 2005-08-02 Pfizer Products Inc. Amides de l'acide 7-¬(4'-trifluoromethylbiphenyl-2-carbonyl)amino|-quinoleine-3-carboxylique et methodes pour inhiber la secretion d'apolipoproteine b
IL139449A0 (en) 1999-11-10 2001-11-25 Pfizer Prod Inc Use of apo b secretion/mtp inhibitors
US20020032238A1 (en) * 2000-07-08 2002-03-14 Henning Priepke Biphenylcarboxylic acid amides, the preparation thereof and the use thereof as medicaments
US6417367B1 (en) * 2000-08-11 2002-07-09 Pfizer Inc. Methods of making quinoline amides
JP2004510763A (ja) 2000-10-05 2004-04-08 藤沢薬品工業株式会社 アポb分泌阻害剤としてのベンズアミド化合物
OA12626A (en) 2001-06-28 2006-06-13 Pfizer Prod Inc triamide-substituted indoles, benzofuranes and benzothiophenes as inhibitors of microsomal triglyceride transfer protein (MTP)and/or apolipoprotein B(APO B) secretion.
EP1447402A4 (fr) * 2001-10-25 2005-01-19 Compose quinoline
AU2002360489A1 (en) * 2001-12-07 2003-06-23 The Regents Of The University Of California Treatment for age-related macular degeneration
US20030162788A1 (en) * 2002-01-10 2003-08-28 Boehringer Ingelheim Pharma Kg Combination of MTP inhibitors or apoB-secretion inhibitors with fibrates for use as pharmaceuticals
US7625948B2 (en) 2002-02-28 2009-12-01 Japan Tobacco Inc. Ester compound and medicinal use thereof
JP2006516028A (ja) * 2002-12-20 2006-06-15 ファイザー・プロダクツ・インク ミクロソームトリグリセリド輸送タンパク質阻害剤
WO2004056777A1 (fr) * 2002-12-20 2004-07-08 Pfizer Products Inc. Inhibiteurs de proteine microsomale de transfert de triglyceride
AP2006003685A0 (en) * 2004-02-04 2006-08-31 Pfizer Prod Inc Substituted quinoline compounds

Also Published As

Publication number Publication date
JP2007520543A (ja) 2007-07-26
SV2007002007A (es) 2007-03-20
US20060223851A1 (en) 2006-10-05
US20070093525A1 (en) 2007-04-26
US7393958B2 (en) 2008-07-01
GEP20084360B (en) 2008-04-29
US20050234099A1 (en) 2005-10-20
CA2555133A1 (fr) 2005-09-01
AP2006003685A0 (en) 2006-08-31
EP1716137A1 (fr) 2006-11-02
TW200533354A (en) 2005-10-16
KR100799802B1 (ko) 2008-01-31
KR20060127123A (ko) 2006-12-11
TWI306454B (en) 2009-02-21
EA010369B1 (ru) 2008-08-29
AU2005214159A1 (en) 2005-09-01
PE20050773A1 (es) 2005-10-26
IL208963A0 (en) 2011-07-31
MA28347A1 (fr) 2006-12-01
US7368573B2 (en) 2008-05-06
BRPI0507462A (pt) 2007-07-10
EA200601239A1 (ru) 2007-02-27
PA8623001A1 (es) 2006-03-24
WO2005080373A1 (fr) 2005-09-01
NL1028192A1 (nl) 2005-08-08
CO5700721A2 (es) 2006-11-30
IL176715A0 (en) 2006-10-31
US7468378B2 (en) 2008-12-23
ECSP066717A (es) 2006-10-31
CR8544A (es) 2006-11-30
AR047529A1 (es) 2006-01-25
TW200906800A (en) 2009-02-16
NO20063928L (no) 2006-10-31
NL1028192C2 (nl) 2006-05-30
UY28734A1 (es) 2005-09-30

Similar Documents

Publication Publication Date Title
OA13365A (en) Substituted quinoline compounds.
AP1388A (en) Nicotinamide derivatives
KR100575919B1 (ko) 미소체 트리글리세라이드 전달 단백질(mtp) 및/또는아포지방단백질 b(apo b)분비의 억제제로서의트리아미드-치환된 인돌, 벤조푸란 및 벤조티오펜
MXPA02009020A (es) Derivados de beta-aminoacidos ciclicos como inhibidores de las metaloproteasas de matriz y factor de necrosis de tumor alfa.
EP1883630A2 (fr) Procedes de synthese de derives de 6-alkylaminoquinoline
JP2001504809A (ja) マトリクス金属プロテナイーゼおよびtaceに対する阻害薬としてのオルト―スルホンアミドアリールヒドロキサム酸の製造および使用
BRPI0809931B1 (pt) antagonistas do receptor do hormônio liberador de gonadotrofina e métodos relacionados com o mesmo
EP2141147A1 (fr) Dérivé de l'ornithine
JP2006514032A (ja) ミクロソームトリグリセリド転送タンパク質阻害剤
WO2004056775A1 (fr) Inhibiteurs de proteine de transfert de triglyceride microsomale
JPH11500436A (ja) 1−アリール−2−アシルアミノ−エタン化合物およびニューロキニン特にニューロキニン1アンタゴニストとしてのそれらの用途
MXPA06007785A (en) Substituted quinoline compounds
JPH05239024A (ja) 縮合複素環カルボン酸誘導体、その製造法、中間体および剤
US20130072519A1 (en) 2-phenyl benzoylamides