[go: up one dir, main page]

CA2420210A1 - Procede stereoselectif pour preparer des derives de cyclohexylamine - Google Patents

Procede stereoselectif pour preparer des derives de cyclohexylamine Download PDF

Info

Publication number
CA2420210A1
CA2420210A1 CA002420210A CA2420210A CA2420210A1 CA 2420210 A1 CA2420210 A1 CA 2420210A1 CA 002420210 A CA002420210 A CA 002420210A CA 2420210 A CA2420210 A CA 2420210A CA 2420210 A1 CA2420210 A1 CA 2420210A1
Authority
CA
Canada
Prior art keywords
compound
formula
optionally substituted
alkyl
appropriate
Prior art date
Legal status (The legal status 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 status listed.)
Abandoned
Application number
CA002420210A
Other languages
English (en)
Inventor
Michael Edward Kobierski
Rui Lin Gu
Charles Jackson Barnett
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Eli Lilly and Co
Original Assignee
Individual
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 Individual filed Critical Individual
Publication of CA2420210A1 publication Critical patent/CA2420210A1/fr
Abandoned legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • 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

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

L'invention concerne un procédé de préparation d'acide (1R,3S)-3-(9-chloro-3-méthyl-4-oxo-5H-(isoxazoloquinoline-5-yl))cyclohexanecarboxylique et d'esters de celui-ci, représentés par les formules II et III. Dans les formules, R représente des groupes alkyle inférieurs, et A et B représentent N ou O, à condition que si A représente N, B représente O, ou si A représente O, B représente N.
CA002420210A 2000-09-22 2001-09-13 Procede stereoselectif pour preparer des derives de cyclohexylamine Abandoned CA2420210A1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US23464900P 2000-09-22 2000-09-22
US60/234,649 2000-09-22
PCT/US2001/026023 WO2002024705A1 (fr) 2000-09-22 2001-09-13 Procede stereoselectif pour preparer des derives de cyclohexylamine

Publications (1)

Publication Number Publication Date
CA2420210A1 true CA2420210A1 (fr) 2002-03-28

Family

ID=22882230

Family Applications (1)

Application Number Title Priority Date Filing Date
CA002420210A Abandoned CA2420210A1 (fr) 2000-09-22 2001-09-13 Procede stereoselectif pour preparer des derives de cyclohexylamine

Country Status (5)

Country Link
EP (1) EP1322652A1 (fr)
JP (1) JP2004509897A (fr)
AU (1) AU2001294518A1 (fr)
CA (1) CA2420210A1 (fr)
WO (1) WO2002024705A1 (fr)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PH12015501678B1 (en) 2009-06-17 2022-07-06 Vertex Pharma Inhibitors of influenza viruses replication
CN102485726B (zh) * 2010-12-02 2015-07-01 天津药明康德新药开发有限公司 一种1-r-1’-螺-(哌啶-4,4’-喹啉)-2’(3’-氢)酮的制备方法
KR20130128436A (ko) 2010-12-16 2013-11-26 버텍스 파마슈티칼스 인코포레이티드 인플루엔자 바이러스 복제의 억제제
RU2013132683A (ru) 2010-12-16 2015-01-27 Вертекс Фармасьютикалз Инкорпорейтед Ингибиторы репликации вирусов гриппа
AU2011343642A1 (en) 2010-12-16 2013-05-02 Vertex Pharmaceuticals Incorporated Inhibitors of influenza viruses replication

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU3468099A (en) * 1998-04-08 1999-10-25 Eli Lilly And Company Methods for inhibiting mrp1
US6369070B1 (en) * 1998-04-08 2002-04-09 Eli Lilly And Company Methods for inhibiting mrp1

Also Published As

Publication number Publication date
WO2002024705A1 (fr) 2002-03-28
AU2001294518A1 (en) 2002-04-02
JP2004509897A (ja) 2004-04-02
EP1322652A1 (fr) 2003-07-02

Similar Documents

Publication Publication Date Title
ES2311992T3 (es) Derivados de quinolina sustituida com,o inhibidores de cinesina mitotica.
EP1250340B1 (fr) Methodes et composes destines a inhiber mrp1
US6369070B1 (en) Methods for inhibiting mrp1
CA2420210A1 (fr) Procede stereoselectif pour preparer des derives de cyclohexylamine
US6673809B2 (en) Tricyclic compounds as MRP1-inhibitors
US20040010005A1 (en) Stereoselective process for preparing cylcohexyl amine derivatives
US6686376B2 (en) Methods and compounds for inhibiting MRP1
KR20010042482A (ko) Mrp1의 억제 방법
KR20170073699A (ko) 신규한 유형의 시티딘 유도체 이량체 및 그의 용도
EP1819704B1 (fr) Derive amide de l'acide pyrrolopyridine-2-carboxylique utile en tant qu'inhibiteur de la glycogene-phosphorylase
EP1067932A1 (fr) Methodes d'inhibition de la mrp1
JP2007534733A (ja) 血管損傷剤として使用する3,4−ジ置換マレイミド
US7101891B2 (en) Compounds and pharmaceutical compositions for inhibiting MRP1
EP1392702B1 (fr) Derives d'oxatriazacyclopentanaphtalene utiles en tant qu'inhibiteurs de mrp1
US7064131B2 (en) Compounds and methods for inhibiting MRP1
CN118772107A (zh) Hdac抑制剂及其用途
CN108822127A (zh) 4-羟亚胺基噻吩并[2,3-b]噻喃-2-甲酰胺类化合物及其用途
KR20070023689A (ko) 유사분열 키네신 억제제로서의 치환 퀴놀린 유도체
MXPA00009814A (en) Methods for inhibiting mrp1
HK1107984B (en) Pyrrolopyridine-2-carboxylic acid amide derivative useful as inhibitor of glycogen phosphorylase

Legal Events

Date Code Title Description
FZDE Dead