Process to obtain 6-O-methylerythromycin a (clarithromycin)_form II
    1.
    发明申请
    Process to obtain 6-O-methylerythromycin a (clarithromycin)_form II 审中-公开
    获得6-O-甲基红霉素a(克拉霉素)的方法II

    公开(公告)号:US20060247427A1

    公开(公告)日:2006-11-02

    申请号:US11491735

    申请日:2006-07-24

    IPC分类号: C07H17/08

    CPC分类号: C07H17/08

    摘要: The present invention provides a process for the preparation of 6-O-methylerythromycin A Form II comprising treating 6-O-methylerythromycin A with organic acid selected form trifluoroacetic acid, para-toluene sulphonic acid, oxalic acid or acetic acid and converting it into an organic salt of 6-O-methylerythromycin A, which can be neutralized by base to give 6-O-methylerythromycin A Form II.

    摘要翻译: 本发明提供了制备6-O-甲基红霉素A形式II的方法,包括用选自三氟乙酸,对甲苯磺酸,草酸或乙酸的有机酸处理6-O-甲基红霉素A,并将其转化为 6-O-甲基红霉素A的有机盐,可通过碱中和得到6-O-甲基红霉素A型II。

    Process for preparing Valsartan
    2.
    发明申请
    Process for preparing Valsartan 失效
    缬沙坦制备方法

    公开(公告)号:US20060258878A1

    公开(公告)日:2006-11-16

    申请号:US11491638

    申请日:2006-07-24

    IPC分类号: C07C255/49

    CPC分类号: C07D257/04 C07C255/58

    摘要: The invention relates to novel compound of formula (IV), which is an organic acid salt of N-[(2′-cyanobiphenyl-4-yl)methyl]-(L)-valine ester. This compound is an useful intermediate for process of preparation of Valsartan of formula (I), chemically known as (S)—N-(1-Carboxy-2-methylprop-1-yl)-N-pentanoyl-N-[2′-(1H-tetrazol-5-yl)biphenyl-4-ylmethyl]amine. This invention also relates to a process for preparing Valsartan using novel intermediate of formula (IV).

    摘要翻译: 本发明涉及新的式(Ⅳ)化合物,它是N - [(2'-氰基联苯-4-基)甲基] - (L) - 缬氨酸酯的有机酸盐。 该化合物是制备式(I)的缬沙坦的方法的有用的中间体,化学上称为(S)-N-(1-羧基-2-甲基丙-1-基)-N-戊酰基-N- [2' - (1H-四唑-5-基)联苯-4-基甲基]胺。 本发明还涉及使用式(IV)的新型中间体制备缬沙坦的方法。