HK1062294A1 - Compounds useful as intermediates for 4-aminoquinoline derivates - Google Patents

Compounds useful as intermediates for 4-aminoquinoline derivates

Info

Publication number
HK1062294A1
HK1062294A1 HK04105255A HK04105255A HK1062294A1 HK 1062294 A1 HK1062294 A1 HK 1062294A1 HK 04105255 A HK04105255 A HK 04105255A HK 04105255 A HK04105255 A HK 04105255A HK 1062294 A1 HK1062294 A1 HK 1062294A1
Authority
HK
Hong Kong
Prior art keywords
aminoquinoline
derivates
intermediates
compounds useful
compounds
Prior art date
Application number
HK04105255A
Other languages
English (en)
Inventor
David Burns Damon
Robert Wayne Dugger
Robert William Scott
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 HK1062294A1 publication Critical patent/HK1062294A1/xx

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00Carboxylic acid nitriles
    • C07C255/01Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms
    • C07C255/24Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms containing cyano groups and singly-bound nitrogen atoms, not being further bound to other hetero atoms, bound to the same saturated acyclic carbon skeleton
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C237/00Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
    • C07C237/02Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
    • C07C237/04Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being acyclic and saturated
    • C07C237/06Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being acyclic and saturated having the nitrogen atoms of the carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C271/00Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
    • C07C271/62Compounds containing any of the groups, X being a hetero atom, Y being any atom, e.g. N-acylcarbamates
    • C07C271/64Y being a hydrogen or a carbon atom, e.g. benzoylcarbamates
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (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)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Vascular Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Cardiology (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Quinoline Compounds (AREA)
  • Steroid Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Peptides Or Proteins (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Plural Heterocyclic Compounds (AREA)
HK04105255A 2001-04-30 2004-07-19 Compounds useful as intermediates for 4-aminoquinoline derivates HK1062294A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US28752201P 2001-04-30 2001-04-30
PCT/IB2002/001217 WO2002088069A2 (en) 2001-04-30 2002-04-08 Compounds useful as intermediates for 4-aminoquinoline derivatives

Publications (1)

Publication Number Publication Date
HK1062294A1 true HK1062294A1 (en) 2004-10-29

Family

ID=23103272

Family Applications (1)

Application Number Title Priority Date Filing Date
HK04105255A HK1062294A1 (en) 2001-04-30 2004-07-19 Compounds useful as intermediates for 4-aminoquinoline derivates

Country Status (25)

Country Link
US (3) US6689897B2 (pl)
EP (2) EP1383734B1 (pl)
JP (2) JP3924251B2 (pl)
KR (2) KR100591998B1 (pl)
CN (3) CN1267411C (pl)
AR (3) AR036331A1 (pl)
AT (2) ATE316957T1 (pl)
AU (1) AU2002253448B2 (pl)
BR (2) BR0209291A (pl)
CA (2) CA2445693A1 (pl)
CZ (2) CZ20032898A3 (pl)
DE (2) DE60210265T2 (pl)
DK (2) DK1425270T3 (pl)
ES (2) ES2256461T3 (pl)
HK (1) HK1062294A1 (pl)
HU (2) HU225777B1 (pl)
IL (2) IL157546A0 (pl)
MX (2) MXPA03009935A (pl)
PL (2) PL366700A1 (pl)
PT (1) PT1425270E (pl)
RU (2) RU2265010C2 (pl)
TW (1) TWI250974B (pl)
WO (2) WO2002088069A2 (pl)
YU (2) YU84303A (pl)
ZA (2) ZA200306600B (pl)

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US6197786B1 (en) * 1998-09-17 2001-03-06 Pfizer Inc 4-Carboxyamino-2-substituted-1,2,3,4-tetrahydroquinolines
US20040002615A1 (en) * 2002-06-28 2004-01-01 Allen David Robert Preparation of chiral amino-nitriles
JP2006021999A (ja) * 2002-07-12 2006-01-26 Kaneka Corp 光学活性β−アミノニトリル化合物およびその対掌体アミド化合物の製造方法
US7504508B2 (en) 2002-10-04 2009-03-17 Millennium Pharmaceuticals, Inc. PGD2 receptor antagonists for the treatment of inflammatory diseases
JP2006508077A (ja) * 2002-10-04 2006-03-09 ミレニアム・ファーマシューティカルズ・インコーポレイテッド 炎症疾患を治療するためのpgd2レセプタアンタゴニスト
US20090181966A1 (en) * 2002-10-04 2009-07-16 Millennium Pharmaceuticals, Inc. PGD2 receptor antagonists for the treatment of inflammatory diseases
WO2004056358A1 (en) 2002-12-20 2004-07-08 Pfizer Products Inc. Dosage forms comprising a cetp inhibitor and an hmg-coa reductase inhibitor
WO2004074255A2 (en) * 2003-02-18 2004-09-02 Takasago International Corporation Method for producing an optically active tetrahydroquinoline
US7223859B2 (en) 2003-03-17 2007-05-29 Pfizer Inc. Method for producing (R)-3-[4-(trifluoromethyl) phenylamino]-pentanoic acid amide derivative
EP1604975A4 (en) * 2003-03-17 2006-11-02 Kaneka Corp PROCESSES FOR PRODUCING (R) -3- 4- (TRIFLUOROMETHYL) -PHENYLAMINO-PENTANAMIDE DERIVATIVES
CN1886124A (zh) 2003-09-26 2006-12-27 日本烟草产业株式会社 抑制残余脂蛋白产生的方法
EP2098512A1 (en) * 2003-10-08 2009-09-09 Eli Lilly & Company Compounds and methods for treating dyslipidemia
WO2005046662A2 (en) * 2003-11-07 2005-05-26 Jj Pharma, Inc. Hdl-boosting combination therapy complexes
UA84749C2 (ru) * 2004-04-07 2008-11-25 Милленниум Фармасьютикалз, Инк. Антагонисты рецептора pgd2 для лечения воспалительных заболеваний
WO2006012093A1 (en) * 2004-06-24 2006-02-02 Eli Lilly And Company Compounds and methods for treating dyslipidemia
DE102004031656A1 (de) * 2004-06-30 2006-01-19 Merck Patent Gmbh Tetrahydrochinoline
US7700774B2 (en) 2004-12-20 2010-04-20 Dr. Reddy's Laboratories Ltd. Heterocyclic compounds and their pharmaceutical compositions
AU2006216713A1 (en) 2005-02-24 2006-08-31 Millennium Pharmaceuticals, Inc. PGD2 receptor antagonists for the treatment of inflammatory diseases
CA2610205A1 (en) * 2005-06-20 2006-12-28 Astrazeneca Ab Process for the production of (alkoxycarbonylamino)alkyl sulfonates
UY30244A1 (es) 2006-03-30 2007-11-30 Tanabe Seiyaku Co Un proceso para preparar derivados de tetrahidroquinolina
DE102006031143A1 (de) * 2006-07-04 2008-01-24 Merck Patent Gmbh Fluortenside
DE102006031151A1 (de) * 2006-07-04 2008-01-10 Merck Patent Gmbh Fluortenside
DE102006031149A1 (de) * 2006-07-04 2008-01-10 Merck Patent Gmbh Fluortenside
DE102006032391A1 (de) * 2006-07-04 2008-01-17 Merck Patent Gmbh Fluortenside
DE102006031262A1 (de) * 2006-07-04 2008-01-10 Merck Patent Gmbh Fluortenside
AR065670A1 (es) 2007-03-09 2009-06-24 Indigene Pharmaceuticals Inc Combinacion de metformina r-(+) lipoato y agentes antihiperlipidemicos para el tratamiento de hiperglucemia diabetica y complicaciones diabeticas
JP2011256110A (ja) * 2008-09-30 2011-12-22 Takeda Chem Ind Ltd ヘキサヒドロピロロキノリンの製造法
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
DK2697207T3 (en) 2011-04-12 2017-03-27 Chong Kun Dang Pharmaceutical Corp 3- (2-ARYL-CYCLOALKENYLMETHYL) -OXAZOLIDIN-2-ON DERIVATIVES AS CHOLESTEROL ESTER-TRANSFER PROTEIN (CETP) INHIBITORS
PT2729142T (pt) 2011-07-08 2018-10-01 Novartis Ag Método de tratamento de aterosclerose em sujeitos com nível elevado de triglicéridos
US9493430B2 (en) 2013-01-31 2016-11-15 Chong Kun Dang Pharmaceutical Corp. Biaryl- or heterocyclic biaryl-substituted cyclohexene derivative compounds as CETP inhibitors
WO2015067405A1 (en) * 2013-11-11 2015-05-14 Lonza Ltd Method for preparation of cyano compounds of the 13th group with a lewis acid
PL3180314T3 (pl) * 2014-08-12 2022-11-21 Newamsterdam Pharma B.V. Sposób wytwarzania syntetycznych związków pośrednich do wytwarzania pochodnych tetrahydrochinoliny
CN105294559B (zh) * 2015-06-24 2017-11-14 厦门法茉维特动物药业有限公司 一种医药中间体4‑氨基喹啉类化合物的合成方法

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1097158B1 (en) 1998-07-10 2006-01-25 Massachusetts Institute Of Technology Ligands for metals and metal-catalyzed processes
GT199900147A (es) 1998-09-17 1999-09-06 1, 2, 3, 4- tetrahidroquinolinas 2-sustituidas 4-amino sustituidas.
US6197786B1 (en) 1998-09-17 2001-03-06 Pfizer Inc 4-Carboxyamino-2-substituted-1,2,3,4-tetrahydroquinolines

Also Published As

Publication number Publication date
AR036331A1 (es) 2004-09-01
BR0209238A (pt) 2004-06-15
CA2445623A1 (en) 2002-11-07
US20030216576A1 (en) 2003-11-20
YU84303A (sh) 2006-05-25
EP1383734A2 (en) 2004-01-28
CN1680292A (zh) 2005-10-12
KR100591998B1 (ko) 2006-06-22
KR20040030603A (ko) 2004-04-09
RU2259355C2 (ru) 2005-08-27
PL366584A1 (pl) 2005-02-07
TWI250974B (en) 2006-03-11
IL157544A0 (en) 2004-03-28
US6689897B2 (en) 2004-02-10
CZ20032898A3 (cs) 2004-07-14
KR20040015200A (ko) 2004-02-18
CN1267411C (zh) 2006-08-02
EP1383734B1 (en) 2006-02-01
HUP0304041A3 (en) 2005-08-29
EP1425270A2 (en) 2004-06-09
WO2002088085A3 (en) 2004-03-25
JP3924250B2 (ja) 2007-06-06
AU2002253448B2 (en) 2007-07-05
AR035963A1 (es) 2004-07-28
WO2002088069A9 (en) 2003-12-04
JP3924251B2 (ja) 2007-06-06
YU84403A (sh) 2006-08-17
DE60210265D1 (de) 2006-05-18
CN1297541C (zh) 2007-01-31
RU2003131871A (ru) 2005-04-10
DK1425270T3 (da) 2006-07-03
CZ20032900A3 (cs) 2004-06-16
RU2265010C2 (ru) 2005-11-27
CN100357265C (zh) 2007-12-26
RU2003131870A (ru) 2005-01-27
DE60209004T2 (de) 2006-09-28
KR100639745B1 (ko) 2006-10-30
US20020177716A1 (en) 2002-11-28
US6600045B2 (en) 2003-07-29
CN1529696A (zh) 2004-09-15
JP2004531541A (ja) 2004-10-14
DK1383734T3 (da) 2006-05-15
MXPA03009935A (es) 2004-01-29
WO2002088069A2 (en) 2002-11-07
ZA200306599B (en) 2004-10-22
PT1425270E (pt) 2006-07-31
ES2259080T3 (es) 2006-09-16
HUP0304039A2 (hu) 2004-03-29
HU225777B1 (en) 2007-08-28
WO2002088069A3 (en) 2003-02-20
HUP0304039A3 (en) 2005-10-28
DE60210265T2 (de) 2006-10-12
JP2004527556A (ja) 2004-09-09
EP1425270B1 (en) 2006-03-29
PL366700A1 (pl) 2005-02-07
US20030073843A1 (en) 2003-04-17
BR0209291A (pt) 2004-07-13
IL157546A0 (en) 2004-03-28
ZA200306600B (en) 2004-08-25
MXPA03009936A (es) 2004-01-29
WO2002088085A2 (en) 2002-11-07
ATE321755T1 (de) 2006-04-15
AR044706A2 (es) 2005-09-21
DE60209004D1 (de) 2006-04-13
US6706881B2 (en) 2004-03-16
ATE316957T1 (de) 2006-02-15
HUP0304041A2 (hu) 2004-04-28
ES2256461T3 (es) 2006-07-16
CA2445693A1 (en) 2002-11-07
CN1505609A (zh) 2004-06-16

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Legal Events

Date Code Title Description
PC Patent ceased (i.e. patent has lapsed due to the failure to pay the renewal fee)

Effective date: 20100408