Process for preparing pyrimidine derivatives
    1.
    发明授权
    Process for preparing pyrimidine derivatives 失效
    嘧啶衍生物的制备方法

    公开(公告)号:US5763608A

    公开(公告)日:1998-06-09

    申请号:US595885

    申请日:1996-02-05

    摘要: The present invention provides a process for preparing a 5,6-dihydro-3H-pyrimidin-4-one derivatives which comprises the steps of (a) dehydrating a N-acyl beta amino acid in the presence of a dehydration agent and an organic solvent for a sufficient period of time and under suitable temperature and pressure conditions to form an oxazone (b) adding a carboxylic acid and a primary amine salt of a carboxylic acid to said oxazone to form a mixture, (c) distilling azeotropically said mixture for a suitable period of time and under suitable temperature and pressure conditions to substantially remove said dehydration agent and said organic solvent, and (d) heating the product of step (c) for a sufficient period of time and under suitable temperature and pressure conditions to form said pyrimidin derivatives.

    摘要翻译: 本发明提供一种制备5,6-二氢-3H-嘧啶-4-酮衍生物的方法,其包括以下步骤:(a)在脱水剂和有机溶剂存在下使N-酰基β氨基酸脱水 (b)向所述恶唑酮中加入羧酸和羧酸的伯胺盐以形成混合物,(c)将共沸蒸馏所述混合物用于 适当的时间段和在合适的温度和压力条件下,以基本上除去所述脱水剂和所述有机溶剂,和(d)在合适的温度和压力条件下加热步骤(c)的产物足够的时间以形成所述 嘧啶衍生物。

    Process for preparing cyclic ketones
    4.
    发明授权
    Process for preparing cyclic ketones 失效
    制备环酮的方法

    公开(公告)号:US5489712A

    公开(公告)日:1996-02-06

    申请号:US334822

    申请日:1994-11-04

    CPC分类号: C07C45/68 C07C45/67

    摘要: The present invention provides a novel process for preparing cyclic ketones, such as indanones, which comprises the steps of (a) subjecting a substituted ketone to suitable methylenation conditions in the presence of a methylene transfer agent and an acylating agent for a sufficient period of time and under suitable conditions of temperature and pressure to form the corresponding alpha, beta unsaturated ketone, and (b) subjecting said unsaturated ketone to suitable cyclization conditions in the presence of a suitable acid or base for a sufficient period of time and under suitable conditions of temperature and pressure to form said cyclic ketones.

    摘要翻译: 本发明提供了一种制备环酮的新方法,如茚满酮,其包括以下步骤:(a)在亚甲基转移剂和酰化剂的存在下使取代的酮进行合适的亚甲基化条件足够的时间 并在适当的温度和压力条件下形成相应的α,β不饱和酮,和(b)在合适的酸或碱存在下将所述不饱和酮在适当的环化条件下充分足够的时间和在适当的条件下 温度和压力以形成所述环酮。