AU2002241271B2 - Method for preparing 7-quinolinyl-3,5-dihydroxyhept-6-enoate - Google Patents

Method for preparing 7-quinolinyl-3,5-dihydroxyhept-6-enoate Download PDF

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Publication number
AU2002241271B2
AU2002241271B2 AU2002241271A AU2002241271A AU2002241271B2 AU 2002241271 B2 AU2002241271 B2 AU 2002241271B2 AU 2002241271 A AU2002241271 A AU 2002241271A AU 2002241271 A AU2002241271 A AU 2002241271A AU 2002241271 B2 AU2002241271 B2 AU 2002241271B2
Authority
AU
Australia
Prior art keywords
formula
aqueous solution
hydrogen peroxide
compound represented
enoate
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.)
Ceased
Application number
AU2002241271A
Other languages
English (en)
Other versions
AU2002241271A1 (en
Inventor
Masami Kozawa
Kenji Suzuki
Kenichi Tokunaga
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.)
Nissan Chemical Corp
Original Assignee
Nissan Chemical Corp
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 Nissan Chemical Corp filed Critical Nissan Chemical Corp
Publication of AU2002241271A1 publication Critical patent/AU2002241271A1/en
Application granted granted Critical
Publication of AU2002241271B2 publication Critical patent/AU2002241271B2/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02—Heterocyclic 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
    • C07D215/12—Heterocyclic 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 substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D215/14—Radicals substituted by oxygen atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Quinoline Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Peptides Or Proteins (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
AU2002241271A 2001-04-05 2002-03-22 Method for preparing 7-quinolinyl-3,5-dihydroxyhept-6-enoate Ceased AU2002241271B2 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2001-106820 2001-04-05
JP2001106820 2001-04-05
PCT/JP2002/002779 WO2002081451A1 (en) 2001-04-05 2002-03-22 Method for preparing 7-quinolinyl-3,5-dihydroxyhept-6-enoate

Publications (2)

Publication Number Publication Date
AU2002241271A1 AU2002241271A1 (en) 2003-04-10
AU2002241271B2 true AU2002241271B2 (en) 2007-01-25

Family

ID=18959261

Family Applications (1)

Application Number Title Priority Date Filing Date
AU2002241271A Ceased AU2002241271B2 (en) 2001-04-05 2002-03-22 Method for preparing 7-quinolinyl-3,5-dihydroxyhept-6-enoate

Country Status (21)

Country Link
US (1) US7038056B2 (enExample)
EP (1) EP1375485B1 (enExample)
JP (1) JP4380160B2 (enExample)
KR (1) KR100838135B1 (enExample)
CN (1) CN1241914C (enExample)
AT (1) ATE506349T1 (enExample)
AU (1) AU2002241271B2 (enExample)
CA (1) CA2442713C (enExample)
CZ (1) CZ20032633A3 (enExample)
DE (1) DE60239793D1 (enExample)
HU (1) HUP0401401A3 (enExample)
IL (2) IL158151A0 (enExample)
MX (1) MXPA03009095A (enExample)
NO (1) NO326089B1 (enExample)
NZ (1) NZ528149A (enExample)
RU (1) RU2260001C2 (enExample)
SK (1) SK287922B6 (enExample)
TW (1) TWI317356B (enExample)
UA (1) UA76984C2 (enExample)
WO (1) WO2002081451A1 (enExample)
ZA (1) ZA200307704B (enExample)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100445267C (zh) * 2005-10-21 2008-12-24 上海医药工业研究院 4-(4-氟-苯基)-3-羟甲基-2-环丙基-喹啉的制备方法
KR101160152B1 (ko) * 2009-02-24 2012-06-27 한미사이언스 주식회사 스타틴 화합물 또는 그 염의 신규 제조방법, 및 이에 사용되는 중간체 화합물

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4248882A (en) * 1980-02-12 1981-02-03 Pfizer Inc. Treating diabetes-associated complications with hydantoin amines
US4645854A (en) * 1985-04-25 1987-02-24 Merck & Co., Inc. Process for preparing HMG-CoA reductase inhibitors with a 3,5-dihydroxypentanoate subunit
EP0164049B1 (en) * 1984-06-04 1990-12-12 Merck & Co. Inc. Process for preparing hmg-coa reductase inhibtors with a 3,5-dihydroxypentanoate subunit
CA1336714C (en) 1987-08-20 1995-08-15 Yoshihiro Fujikawa Quinoline type mevalonolactone inhibitors of cholesterol biosynthesis
JP2569746B2 (ja) * 1987-08-20 1997-01-08 日産化学工業株式会社 キノリン系メバロノラクトン類
US5753675A (en) * 1989-03-03 1998-05-19 Novartis Pharmaceuticals Corporation Quinoline analogs of mevalonolactone and derivatives thereof
JP3528186B2 (ja) * 1991-06-24 2004-05-17 日産化学工業株式会社 光学活性キノリンメバロン酸のジアステレオマー塩
JP3130342B2 (ja) * 1991-10-04 2001-01-31 日産化学工業株式会社 動脈硬化性血管内膜肥厚抑制薬
JP3554036B2 (ja) 1994-09-06 2004-08-11 宇部興産株式会社 光学活性な７−置換キノリル−３，５−ジヒドロキシ−ヘプト−６−エン酸エステル誘導体の製造方法
AU755543B2 (en) 1997-12-19 2002-12-12 Warner-Lambert Export Limited Process for the synthesis of 1,3-diols
JP4236463B2 (ja) * 2000-10-13 2009-03-11 ダイセル化学工業株式会社 光学活性な（３ｒ，５ｓ，６ｅ）−７−［２−シクロプロピル−４−（４−フルオロフェニル）キノリン−３−イル］−３，５−ジヒドロキシ−６−ヘプテン酸エチルの製造方法
EP1365029A4 (en) * 2001-02-02 2009-07-29 Mitsubishi Chem Corp "PROCESS FOR PREPARING (3R, 5S) - (E) -7-2-CYCLOPROPYL-4- (4-FLUORPHENYL) CHINOLINE-3-YL-3,5-DIHYDROXY-HEPT-6-ACID ESTERS"

Also Published As

Publication number Publication date
CA2442713C (en) 2010-05-18
IL158151A (en) 2009-09-22
RU2003132440A (ru) 2005-01-10
SK287922B6 (sk) 2012-04-03
NZ528149A (en) 2005-05-27
NO20034438L (no) 2003-10-03
NO326089B1 (no) 2008-09-15
SK12372003A3 (sk) 2004-04-06
JP4380160B2 (ja) 2009-12-09
EP1375485A1 (en) 2004-01-02
EP1375485B1 (en) 2011-04-20
KR20030086342A (ko) 2003-11-07
CZ20032633A3 (cs) 2003-12-17
UA76984C2 (en) 2006-10-16
MXPA03009095A (es) 2004-02-12
ATE506349T1 (de) 2011-05-15
TWI317356B (enExample) 2009-11-21
ZA200307704B (en) 2004-10-04
CA2442713A1 (en) 2002-10-17
WO2002081451A1 (en) 2002-10-17
JPWO2002081451A1 (ja) 2004-07-29
US20050014947A1 (en) 2005-01-20
CN1241914C (zh) 2006-02-15
DE60239793D1 (de) 2011-06-01
EP1375485A4 (en) 2005-03-23
HUP0401401A3 (en) 2012-05-02
CN1500079A (zh) 2004-05-26
HUP0401401A2 (hu) 2004-12-28
IL158151A0 (en) 2004-03-28
NO20034438D0 (no) 2003-10-03
KR100838135B1 (ko) 2008-06-13
RU2260001C2 (ru) 2005-09-10
US7038056B2 (en) 2006-05-02

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Date Code Title Description
FGA Letters patent sealed or granted (standard patent)
MK14 Patent ceased section 143(a) (annual fees not paid) or expired