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    • 4. 发明申请
    • Process for the stereoselective preparation of (-)-halofenate and derivatives thereof
    • ( - ) - 卤代苯甲酸酯及其衍生物的立体选择性制备方法
    • US20070072858A1
    • 2007-03-29
    • US11525200
    • 2006-09-20
    • Yan ZhuPeng ChengXin ChenJingyuan MaZuchun Zhao
    • Yan ZhuPeng ChengXin ChenJingyuan MaZuchun Zhao
    • A61K31/5375A61K31/495A61K31/4025A61K31/401
    • C07D295/185
    • The present invention provides a compounds the formula (IV): and methods for producing an α-(phenoxy)phenylacetic acid compound of the formula: wherein R1 is a member selected from the group consisting of: each R2 is a member independently selected from the group consisting of (C1-C4)alkyl, halo, (C1-C4)haloalkyl, amino, (C1-C4)aminoalkyl, amido, (C1-C4)amidoalkyl, (C1-C4)sulfonylalkyl, (C1-C4)sulfamylalkyl, (C1-C4)alkoxy, (C1-C4)heteroalkyl, carboxy and nitro; the subscript n is 1 when R1 has the formula (a) or (b) and 2 when R1 has the formula (c) or (d); the subscript m is an integer of from 0 to 3; * indicates a carbon which is enriched in one stereoisomeric configuration; and the wavy line indicates the point of attachment of R1; and compounds
    • 本发明提供式(IV)化合物及其制备下式的α-(苯氧基)苯乙酸化合物的方法:其中R 1是选自以下的成员:各 R 2是独立地选自(C 1 -C 4 -C 4)烷基,卤素,(C 1 -C 4)烷基的成员, C 1 -C 4卤代烷基,氨基,(C 1 -C 4)氨基烷基,酰氨基,(C 1 H 4) (C 1 -C 4)磺酰基烷基,(C 1 -C 4)磺酰基烷基,(C 1 -C 4 - C 1 -C 4亚磺酰基烷基,(C 1 -C 4 -C 4)烷氧基,(C 1 -C 3 - 亚磺酰基烷基) > 4个)杂烷基,羧基和硝基; 当R 1具有式(a)或(b)时,下标n为1,当R 1具有式(c)或(d))时,下标n为1。 下标m为0〜3的整数; *表示富含一种立体异构构型的碳; 波浪线表示R 1的连接点; 和化合物