Process for purifying n2-(1(s)-ethoxycarbonyl-3-phenylpropyl)-n6-thifluoroacetyl-l-lysine
    21.
    发明授权
    Process for purifying n2-(1(s)-ethoxycarbonyl-3-phenylpropyl)-n6-thifluoroacetyl-l-lysine 失效
    纯化N2-(1(s) - 乙氧基羰基-3-苯基丙基)-n6-三氟乙酰基-1-赖氨酸的方法

    公开(公告)号:US07253299B2

    公开(公告)日:2007-08-07

    申请号:US10432288

    申请日:2002-07-10

    IPC分类号: C07C229/00 C07C51/42

    CPC分类号: C07C231/24 C07C233/47

    摘要: A process for purifying N2-(1(S)-ethoxycarbonyl-3-phenylpropyl)-N6-trifluoroacetyl-L-lysine which comprises subjecting N2-(1(S)-ethoxycarbonyl-3-phenylpropyl)-N6-trifluoroacetyl-L-lysine contaminated with impurities to crystallization from a solvent comprising a water-soluble non-protic organic solvent, thereby removing the impurities into the mother liquor and giving crystals of N2-(1(S)-ethoxycarbonyl-3-phenylpropyl)-N6-trifluoroacetyl-L-lysine, according to which N2-(1(S)-ethoxycarbonyl-3-phenylpropyl)-N6-trifluoroacetyl-L-lysine having a high quality can be obtained in a high yield and a high productivity and which is suitable for practice on an industrial scale.

    摘要翻译: 一种纯化N 2 - (1(S) - 乙氧基羰基-3-苯基丙基)-N 6 - 三氟乙酰基-L-赖氨酸的方法,其包括使N 2 - 被杂质污染的(1(S) - 乙氧基羰基-3-苯基丙基)-N 6 - 三氟乙酰基-L-赖氨酸从包含水溶性非质子有机物 溶剂,从而将杂质除去到母液中,得到N 2 - (1(S) - 乙氧基羰基-3-苯基丙基)-N 6 - 三氟乙酰基-L - 赖氨酸,其中具有高质量的N 2 - (1(S) - 乙氧基羰基-3-苯基丙基)-N 6 - 三氟乙酰基-L-赖氨酸可以是 以高产量和高生产率获得,适用于工业规模的实践。

    Processes for producing .alpha.-halo ketones, .alpha.-halohydrins and
epoxides
    22.
    发明授权
    Processes for producing .alpha.-halo ketones, .alpha.-halohydrins and epoxides 失效
    制备α-卤代酮,α-卤代醇和环氧化物的方法

    公开(公告)号:US5929284A

    公开(公告)日:1999-07-27

    申请号:US722102

    申请日:1996-12-18

    摘要: Processes for efficiently producing .alpha.-halo ketones, .alpha.-halohydrins and epoxides on an industrial scale. The prosesses include one for producing an .alpha.-halo ketone of general formula (3) by decarboxylating a product of reaction between a carboxilic acid derivative of general formula (1) and a metal enolate prepared from an .alpha.-haloacetic acid of general formula (2) or an acceptable salt thereof, one for producing an by reducing the .alpha.-halo ketone (3), and one for producing an epoxide (13) by treating the .alpha.-halohydrin (11) with a base to effect ring closure. The above prosesses are particularly suitable for producing optically active .alpha.-halo ketones, .alpha.-halohydrins and epoxides from the corresponding .alpha.-amino acid derivatives. ##STR1##

    摘要翻译: PCT No.PCT / JP96 / 00212 Sec。 371日期:1996年12月18日 102(e)1996年12月18日日期PCT 1996年2月2日PCT PCT。 第WO96 / 23756号公报 日期1996年8月8日工业规模高效生产α-卤代酮,α-卤代醇和环氧化物的方法。 前药包括通过使通式(1)的羧酸衍生物与由通式(2)的α-卤代乙酸制备的金属烯醇化物脱羧的方法来制备通式(3)的α-卤代酮, )或其可接受的盐,其中通过用碱来还原α-卤代酮(3)和通过用碱处理α-卤代醇(11)来制备环氧化物(13)来制备,以实现闭环。 上述产品特别适用于从相应的α-氨基酸衍生物制备光学活性的α-卤代酮,α-卤代醇和环氧化物。