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Title:
PROCESS FOR PRODUCING OPTICALLY ACTIVE 7−&lcub 2−CYCLOPROPYL−4−&lpar 4−FLUOROPHENYL&rpar QUINOLIN−3−YL&rcub −3,5−DIHYDROXYHEPT−6−ENOIC ACID ESTER
Document Type and Number:
WIPO Patent Application WO/2003/027073
Kind Code:
A1
Abstract:
A (3R,5S)−7−&lcub 2−cyclopropyl−4−(4−fluorophenyl)quinolin−3−yl&rcub −3,5−dihydroxyhept−6−enoic acid ester useful as an intermediate for an HMG−CoA reductase inhibitor (cholesterol−lowering agent) can be obtained in a high yield by a method in which a salt of (3R,5S)−7−&lcub 2−cyclopropyl−4−(4−fluorophenyl)quinolin−3−yl&rcub −3,5−dihydroxyhept−6−enoic acid with an amine is reacted with an alcohol in a solvent in the presence of an acid or by a method comprising reacting the salt with an esterifying agent in a solvent in the presence of a base.

Inventors:
NISHINO SHIGEYOSHI (JP)
MATSUSHITA AKIO (JP)
YOKOYAMA SHUJI (JP)
KAWACHI YASUHIRO (JP)
SASAKI HIROSHI (JP)
Application Number:
PCT/JP2002/009638
Publication Date:
April 03, 2003
Filing Date:
September 19, 2002
Export Citation:
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Assignee:
UBE INDUSTRIES (JP)
NISHINO SHIGEYOSHI (JP)
MATSUSHITA AKIO (JP)
YOKOYAMA SHUJI (JP)
KAWACHI YASUHIRO (JP)
SASAKI HIROSHI (JP)
International Classes:
C07D215/14; (IPC1-7): C07D215/14
Foreign References:
EP0520406A11992-12-30
JPH0892217A1996-04-09
Other References:
SUZUKI MIKIO ET AL.: "First systematic chiral syntheses of two pairs of enantiomers with 3,5-dihydroxyheptenoic acid chain, associated with a potent synthetic statin NK-104", BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, vol. 9, no. 20, 1999, pages 2977 - 2982, XP004180521
Attorney, Agent or Firm:
Yanagawa, Yasuo (2-14 Yotsuy, Shinjuku-ku Tokyo, JP)
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