PROCESS FOR THE SYNTHESIS OF ENANTIOMERIC INDANYLAMINE DERIVATIVES
    1.
    发明申请
    PROCESS FOR THE SYNTHESIS OF ENANTIOMERIC INDANYLAMINE DERIVATIVES 失效
    合成苯胺衍生物的方法

    公开(公告)号:US20080200720A1

    公开(公告)日:2008-08-21

    申请号:US12103310

    申请日:2008-04-15

    IPC分类号: C07C271/42

    摘要: A process for manufacturing (R)-propynylaminoindans, and alternatively, a process for manufacturing (S)-propynylaminoindans. The chiral propynylaminoindans include alkoxy or alkylcarbamates derivatives. The process comprises transfer or pressure hydrogenation in the presence of an optically active catalyst to reduce 1-indanones. The chiral product, either (S)- or (R)-indanols undergo nucleophilic substitution to produce the named product. In an additional aspect, the invention relates to novel intermediates and compounds, namely, substituted indanones, substituted (S)-indanols and substituted (R)-indanols.

    摘要翻译: 制备(R) - 丙炔基氨基茚满的方法,或者,制备(S) - 丙炔基氨基茚满的方法。 手性丙炔基氨基茚满包括烷氧基或烷基氨基甲酸酯衍生物。 该方法包括在光学活性催化剂存在下转移或加压氢化以还原1-茚满酮。 (S) - 或(R) - 茚满醇的手性产物经历亲核取代以产生命名的产物。 在另一方面,本发明涉及新的中间体和化合物,即取代的茚满酮,取代的(S) - 茚满醇和取代的(R) - 茚满醇。

    Process for the synthesis of enantiomeric indanylamine derivatives
    2.
    发明授权
    Process for the synthesis of enantiomeric indanylamine derivatives 失效
    合成对映异构茚满胺衍生物的方法

    公开(公告)号:US07476757B2

    公开(公告)日:2009-01-13

    申请号:US12103310

    申请日:2008-04-15

    IPC分类号: C07C261/00

    摘要: A process for manufacturing (R)-propynylaminoindans, and alternatively, a process for manufacturing (S)-propynylaminoindans. The chiral propynylaminoindans include alkoxy or alkylcarbamates derivatives. The process comprises transfer or pressure hydrogenation in the presenc of an optically active catalyst to reduce 1-indanones. The chiral product, either (S)- or (R)-indanols undergo nucleophilic substitution to produce the named product. In an additional aspect, the invention relates to novel intermediates and compounds, namely, substituted indanones, substituted (S)-indanols and substituted (R)-indanols.

    摘要翻译: 制备(R) - 丙炔基氨基茚满的方法,或者,制备(S) - 丙炔基氨基茚满的方法。 手性丙炔基氨基茚满包括烷氧基或烷基氨基甲酸酯衍生物。 该方法包括在光学活性催化剂的存在下转移或加压氢化以还原1-茚满酮。 (S) - 或(R) - 茚满醇的手性产物经历亲核取代以产生命名的产物。 在另一方面,本发明涉及新的中间体和化合物,即取代的茚满酮,取代的(S) - 茚满醇和取代的(R) - 茚满醇。

    Process for the synthesis of enantiomeric indanylamine derivatives
    3.
    发明授权
    Process for the synthesis of enantiomeric indanylamine derivatives 失效
    合成对映异构茚满胺衍生物的方法

    公开(公告)号:US07375249B2

    公开(公告)日:2008-05-20

    申请号:US11358995

    申请日:2006-02-21

    IPC分类号: C07C211/00

    摘要: A process for manufacturing (R)-propynylaminoindans, and alternatively, a process for manufacturing (S)-propynylaminoindans. The chiral propynylaminoindans include alkoxy or alkylcarbamates derivatives. The process comprises transfer or pressure hydrogenation in the presence of an optically active catalyst to reduce 1-indanones. The chiral product, either (S)- or (R)-indanols undergo nucleophilic substitution to produce the named product. In an additional aspect, the invention relates to novel intermediates and compounds, namely, substituted indanones, substituted (S)-indanols and substituted (R)-indanols.

    摘要翻译: 制备(R) - 丙炔基氨基茚满的方法,或者,制备(S) - 丙炔基氨基茚满的方法。 手性丙炔基氨基茚满包括烷氧基或烷基氨基甲酸酯衍生物。 该方法包括在光学活性催化剂存在下转移或加压氢化以还原1-茚满酮。 (S) - 或(R) - 茚满醇的手性产物经历亲核取代以产生命名的产物。 在另一方面,本发明涉及新的中间体和化合物,即取代的茚满酮,取代的(S) - 茚满醇和取代的(R) - 茚满醇。