HUP0004747A2 - 2-es helyzetben helyettesített 4-karboxamino-1,2,3,4,-tetrahidrokinolin-származékok és eljárás előállításukra - Google Patents

2-es helyzetben helyettesített 4-karboxamino-1,2,3,4,-tetrahidrokinolin-származékok és eljárás előállításukra

Info

Publication number
HUP0004747A2
HUP0004747A2 HU0004747A HUP0004747A HUP0004747A2 HU P0004747 A2 HUP0004747 A2 HU P0004747A2 HU 0004747 A HU0004747 A HU 0004747A HU P0004747 A HUP0004747 A HU P0004747A HU P0004747 A2 HUP0004747 A2 HU P0004747A2
Authority
HU
Hungary
Prior art keywords
trifluoromethyl
ethyl
quinoline
dihydro
carboxylic acid
Prior art date
Application number
HU0004747A
Other languages
English (en)
Inventor
David Burns Damon
Robert Wyane Dugger
Original Assignee
Pfizer Products 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 Products Inc. filed Critical Pfizer Products Inc.
Publication of HU0004747D0 publication Critical patent/HU0004747D0/hu
Publication of HUP0004747A2 publication Critical patent/HUP0004747A2/hu
Publication of HUP0004747A3 publication Critical patent/HUP0004747A3/hu

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
    • C07D215/38Nitrogen atoms
    • C07D215/42Nitrogen atoms attached in position 4
    • 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
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Obesity (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Vascular Medicine (AREA)
  • Cardiology (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Urology & Nephrology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Quinoline Compounds (AREA)
  • Steroid Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

A találmány szerinti 2-es helyzetben helyettesített 4-karboxiamino-1,2,3,4-tetrahidrokinolinszármazékok koleszteril-észtertranszportproteint gátló anyagok, ezáltal alkalmasak ateroszkleróziskezelésére. A találmány tárgyköréhez tartoznak továbbá a (-)-(2R,4L) -{[3,5-bisz(trifluormetil)benzil]metoxikarbonilamino}-2-etil-6-trifluormetil-3,4-dihidro-2H-kinolin-1-karbonsav-etil-észter, a (-)-(2R,4S)- 4-[3,5-bisz(trifluormetil)benzilamino]-2-etil-6-trifluormetil-3,4-dihidro-2H-kinolin-1-karbonsav-etil-észter-4-toluolszulfonát, a cisz-4-amino-2-etil-6-trifluormetil-3,4-dihidro-2H-kinolin-1-karbonsav-etil-észter, a cisz-(2-etil-6-trifluormetil-1,2,3,4-tetrahidrokinolin-4-il)-karbaminsav-R1-észter - ahol R1jelentése benzil-, terc-butil- vagy alkilcsoport - és a (-)-(2R,4S)-4-{[3,5-bisz(trifluormetil)benzil] metoxikarbonilamino} -2-etil-6-trifluormetil-3,4-dihidro-2H-kinolin-1-karbonsav-etil-észterelőállítására szolgáló eljárások. Ó
HU0004747A 1999-11-30 2000-11-29 4-carboxyamino-2-substituted-1,2,3,4-tetrahydroquinoline derivatives and process for their preparation HUP0004747A3 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US16796799P 1999-11-30 1999-11-30

Publications (3)

Publication Number Publication Date
HU0004747D0 HU0004747D0 (hu) 2001-02-28
HUP0004747A2 true HUP0004747A2 (hu) 2001-10-28
HUP0004747A3 HUP0004747A3 (en) 2002-12-28

Family

ID=22609556

Family Applications (1)

Application Number Title Priority Date Filing Date
HU0004747A HUP0004747A3 (en) 1999-11-30 2000-11-29 4-carboxyamino-2-substituted-1,2,3,4-tetrahydroquinoline derivatives and process for their preparation

Country Status (45)

Country Link
US (1) US6313142B1 (hu)
EP (1) EP1125929B1 (hu)
JP (1) JP3579345B2 (hu)
KR (1) KR100408177B1 (hu)
CN (1) CN1173953C (hu)
AP (1) AP2000002011A0 (hu)
AR (1) AR029775A1 (hu)
AT (1) ATE315028T1 (hu)
AU (1) AU784694B2 (hu)
BG (1) BG105009A (hu)
BR (1) BR0005636A (hu)
CA (1) CA2327029C (hu)
CO (1) CO5261552A1 (hu)
CY (1) CY1104989T1 (hu)
CZ (1) CZ20004407A3 (hu)
DE (1) DE60025317T2 (hu)
DK (1) DK1125929T3 (hu)
DZ (1) DZ3079A1 (hu)
EA (1) EA003668B1 (hu)
EE (1) EE200000659A (hu)
ES (1) ES2254109T3 (hu)
GE (1) GEP20022798B (hu)
GT (1) GT200000190A (hu)
HK (1) HK1038007A1 (hu)
HN (1) HN2000000203A (hu)
HR (1) HRP20000804A2 (hu)
HU (1) HUP0004747A3 (hu)
ID (1) ID28489A (hu)
IL (1) IL139849A (hu)
IS (1) IS5715A (hu)
MA (1) MA25223A1 (hu)
NO (1) NO20006039L (hu)
NZ (1) NZ508509A (hu)
OA (1) OA11494A (hu)
PA (1) PA8503801A1 (hu)
PE (1) PE20010913A1 (hu)
PL (1) PL344208A1 (hu)
SG (1) SG102603A1 (hu)
SK (1) SK17792000A3 (hu)
TN (1) TNSN00230A1 (hu)
TW (1) TW591016B (hu)
UA (1) UA65615C2 (hu)
UY (1) UY26451A1 (hu)
YU (1) YU71500A (hu)
ZA (1) ZA200006947B (hu)

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HN2000000203A (es) * 1999-11-30 2001-06-13 Pfizer Prod Inc Procedimiento para la obtencion de 1,2,3,4-tetrahidroquinolinas 4-carboxiamino-2- sustituidas.
WO2003053359A2 (en) 2001-12-19 2003-07-03 Atherogenics, Inc. 1,3-bis-(substituted-phenyl)-2-propyn-1-ones and their use to treat disorders
HUP0500165A2 (en) * 2001-12-19 2006-09-28 Atherogenics Inc Chalcone derivatives and their use to treat diseases
US7279297B2 (en) * 2002-04-11 2007-10-09 Roar Holding Llc Ex vivo method for determination of CETP activity and efficacy of heart disease treatment
BR0315041A (pt) * 2002-10-04 2005-08-16 Millennium Pharm Inc Métodos para inibir crth2 em um indivìduo que necessita inibição de crth2; composto; e composição farmacêutica
US7504508B2 (en) * 2002-10-04 2009-03-17 Millennium Pharmaceuticals, Inc. PGD2 receptor antagonists for the treatment of inflammatory diseases
US20090181966A1 (en) * 2002-10-04 2009-07-16 Millennium Pharmaceuticals, Inc. PGD2 receptor antagonists for the treatment of inflammatory diseases
US7223870B2 (en) * 2002-11-01 2007-05-29 Pfizer Inc. Methods for preparing N-arylated oxazolidinones via a copper catalyzed cross coupling reaction
AU2003303239A1 (en) * 2002-12-19 2004-07-14 Atherogenics, Inc. Process of making chalcone derivatives
US20040132771A1 (en) * 2002-12-20 2004-07-08 Pfizer Inc Compositions of choleseteryl ester transfer protein inhibitors and HMG-CoA reductase inhibitors
AU2003283769A1 (en) 2002-12-20 2004-07-14 Pfizer Products Inc. Dosage forms comprising a cetp inhibitor and an hmg-coa reductase inhibitor
JP2006523218A (ja) * 2003-03-04 2006-10-12 高砂香料工業株式会社 光学活性アミン類の製造方法
MXPA05009848A (es) * 2003-03-17 2005-12-06 Japan Tobacco Inc Composiciones farmaceuticas de inhibidores de la proteina de transferencia del ester de colesterilo.
AU2004222436A1 (en) * 2003-03-17 2004-09-30 Japan Tobacco Inc. Method for increasing the oral bioavailability of S-(2-(((1- (2-ethylbutyl) cyclohexyl)carbonyl) amino) phenyl)-2-methylpropanethioate
TWI494102B (zh) * 2003-05-02 2015-08-01 Japan Tobacco Inc 包含s-〔2(〔〔1-(2-乙基丁基)環己基〕羰基〕胺基)苯基〕2-甲基丙烷硫酯及hmg輔酶a還原酶抑制劑之組合
KR20060085675A (ko) * 2003-10-08 2006-07-27 일라이 릴리 앤드 캄파니 이상지혈증 치료를 위한 화합물 및 방법
UA90269C2 (ru) * 2004-04-02 2010-04-26 Мицубиси Танабе Фарма Корпорейшн Тетрагидрохинолиновые производные и способ их получения
EA200700119A1 (ru) * 2004-06-24 2007-10-26 Эли Лилли Энд Компани Соединения и способы лечения дислипидемии
DOP2005000123A (es) 2004-07-02 2011-07-15 Merck Sharp & Dohme Inhibidores de cetp
WO2006033001A1 (en) * 2004-09-23 2006-03-30 Pfizer Products Inc. Quinoline compounds
US7700774B2 (en) * 2004-12-20 2010-04-20 Dr. Reddy's Laboratories Ltd. Heterocyclic compounds and their pharmaceutical compositions
ZA200707498B (en) * 2005-02-24 2008-11-26 Millennium Pharm Inc PGD2 receptor antagonists for the treatment of inflammatory diseases
TW200808731A (en) 2006-03-30 2008-02-16 Tanabe Seiyaku Co A process for preparing tetrahydroquinoline derivatives
CL2008000684A1 (es) 2007-03-09 2008-08-01 Indigene Pharmaceuticals Inc Composicion farmaceutica que comprende metformina r-(+) lipoato y un inhibidor de reductasa hmg-coa; formulacion de dosis unitaria; y uso en el tratamiento de una complicacion diabetica.
CN101429160B (zh) * 2007-11-06 2011-10-19 上海药明康德新药开发有限公司 一种1-r-4-氨基-1,2,3,4-四氢喹啉的合成方法
TWI450896B (zh) 2009-06-30 2014-09-01 Lilly Co Eli 反式-4-〔〔(5s)-5-〔〔〔3,5-雙(三氟甲基)苯基〕甲基〕(2-甲基-2h-四唑-5-基)胺基〕-2,3,4,5-四氫-7,9-二甲基-1h-1-苯并氮呯-1-基〕甲基〕-環己基羧酸
TW202409008A (zh) 2022-07-05 2024-03-01 荷蘭商新阿姆斯特丹製藥公司 奧比特拉(obicetrapib)鹽及彼等之製造方法與中間體

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US6197786B1 (en) 1998-09-17 2001-03-06 Pfizer Inc 4-Carboxyamino-2-substituted-1,2,3,4-tetrahydroquinolines
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Also Published As

Publication number Publication date
CZ20004407A3 (cs) 2002-06-12
JP3579345B2 (ja) 2004-10-20
PL344208A1 (en) 2001-06-04
EA003668B1 (ru) 2003-08-28
ATE315028T1 (de) 2006-02-15
EE200000659A (et) 2001-08-15
JP2001163859A (ja) 2001-06-19
CY1104989T1 (el) 2010-03-03
CA2327029C (en) 2005-08-09
NZ508509A (en) 2001-06-29
GT200000190A (es) 2002-04-27
SK17792000A3 (sk) 2002-10-08
ES2254109T3 (es) 2006-06-16
TW591016B (en) 2004-06-11
US6313142B1 (en) 2001-11-06
SG102603A1 (en) 2004-03-26
KR100408177B1 (ko) 2003-12-01
KR20010052012A (ko) 2001-06-25
ZA200006947B (en) 2002-05-27
NO20006039D0 (no) 2000-11-29
YU71500A (sh) 2003-02-28
HN2000000203A (es) 2001-06-13
AU7178900A (en) 2001-05-31
HK1038007A1 (en) 2002-03-01
IS5715A (is) 2001-05-31
EA200001129A2 (ru) 2001-06-25
PE20010913A1 (es) 2001-09-10
AR029775A1 (es) 2003-07-16
NO20006039L (no) 2001-05-31
BG105009A (en) 2001-11-30
BR0005636A (pt) 2001-07-17
CA2327029A1 (en) 2001-05-30
DZ3079A1 (fr) 2004-10-24
EP1125929A1 (en) 2001-08-22
MA25223A1 (fr) 2001-07-02
HUP0004747A3 (en) 2002-12-28
IL139849A (en) 2006-10-31
DE60025317D1 (de) 2006-03-30
UA65615C2 (uk) 2004-04-15
TNSN00230A1 (fr) 2005-11-10
EA200001129A3 (ru) 2001-10-22
PA8503801A1 (es) 2002-07-30
CN1302800A (zh) 2001-07-11
OA11494A (en) 2004-05-07
EP1125929B1 (en) 2006-01-04
ID28489A (id) 2001-05-31
DE60025317T2 (de) 2006-08-03
HU0004747D0 (hu) 2001-02-28
CN1173953C (zh) 2004-11-03
AU784694B2 (en) 2006-06-01
GEP20022798B (en) 2002-09-25
CO5261552A1 (es) 2003-03-31
IL139849A0 (en) 2002-02-10
AP2000002011A0 (en) 2000-12-31
UY26451A1 (es) 2001-06-29
HRP20000804A2 (en) 2001-06-30
DK1125929T3 (da) 2006-04-03

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