发明名称 Intermediates and process for producing fluorine-containing amino acid compound by using the same.
摘要 The present inventions relate to a (1S,5R,6S)- or (1SR,5RS,6SR)-3-fluoro-2-oxobicycloÄ3.1.0Ühex-3-ene-6-carboxylic acid derivative represented by Formula (1): <CHEM> Äin the formula, R represents OR<1> or NR<1>R<2>, wherein R<1> and R<2> are identical or different, and each represents a hydrogen atom, a C1-C6 alkyl group, a C3-C6 cycloalkyl group, a (C3-C6 cycloalkyl) (C1-C6 alkyl) group, an aryl group, an aryl (C1-C6 alkyl) group, a (C1-C6 alkoxy) (C1-C6 alkyl) group, a C1-C6 hydroxyalkyl group, a (C1-C6 alkylthio) (C1-C6 alkyl) group, or a C1-C6 mercaptoalkyl groupÜ, and a process for producing the same, and a process for efficiently producing a fluorine-containing amino acid compound acting on group 2 metabotropic glutamate receptors, which has treatment effects or prevention effects on psychiatric diseases or neurological diseases, characterized by hydrogenating the derivative, and subsequently, subjecting it to hydantoination or aminocyanidation, followed by hydrolysis.
申请公布号 HK1047430(A1) 申请公布日期 2005.06.10
申请号 HK20020108913 申请日期 2002.12.06
申请人 TAISHO PHARMACEUTICAL CO., LTD. 发明人 ATSURO NAKAZATO;TOSHIHITO KUMAGAI;KAZUNARI SAKAGAMI;KAZUYUKI TOMISAWA;HISANAKA ITO;TAKEO TAGUCHI
分类号 C07C62/38;C07C51/363;C07C67/307;C07C69/757;C07C227/18;C07C227/24;C07C227/26;C07C229/50;C07C231/12;C07C235/82;C07C255/47;C07D235/02;C07D303/42;C07D303/46;(IPC1-7):C07C 主分类号 C07C62/38
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