METHOD FOR PRODUCING BIARYL COMPOUND
    1.
    发明申请
    METHOD FOR PRODUCING BIARYL COMPOUND 有权
    生产二元化合物的方法

    公开(公告)号:US20150239853A1

    公开(公告)日:2015-08-27

    申请号:US14424912

    申请日:2013-08-30

    申请人: API CORPORATION

    发明人: Masahiko Seki

    摘要: The invention provides a production method of a biaryl compound of the formula [3] or a salt thereof, including reacting a 2-phenylazole derivative of the formula [1] or a salt thereof, with a benzene derivative of the formula [2] or a salt thereof in the presence of a metal catalyst, a base, and one or more of (a) a monocarboxylic acid metal salt, (b) a dicarboxylic acid metal salt, (c) a sulfonic acid metal salt, and (d) a phosphate or phosphoric amide metal salt represented by RAxP(O)(OM)y wherein each symbol is as defined herein.

    摘要翻译: 本发明提供式[3]的联芳基化合物或其盐的制备方法,包括使式[1]的2-苯基唑衍生物或其盐与式[2]的苯衍生物或 (a)一元羧酸金属盐,(b)二羧酸金属盐,(c)磺酸金属盐和(d)一种或多种金属催化剂,碱, 由RAxP(O)(OM)y表示的磷酸酯或磷酰胺金属盐,其中每个符号如本文所定义。

    DEPROTECTION METHOD FOR TETRAZOLE COMPOUND
    2.
    发明申请
    DEPROTECTION METHOD FOR TETRAZOLE COMPOUND 有权
    四唑化合物的去保护方法

    公开(公告)号:US20150239854A1

    公开(公告)日:2015-08-27

    申请号:US14429257

    申请日:2013-09-26

    申请人: API CORPORATION

    发明人: Masahiko Seki

    摘要: The present invention relates to a method of deprotecting a tetrazole compound, useful as an intermediate for angiotensin II receptor blockers, and provides a novel production method of angiotensin II receptor blockers.Provided is a production method of a compound represented by the formula [3] or [4] or a salt thereof, including (i) reducing a compound represented by the formula [1] or [2] or a salt thereof in the presence of a metal catalyst and an alkaline earth metal salt, or (ii) reacting the compound with a particular amount of Brønsted acid: wherein each symbol is as defined in the present specification.

    摘要翻译: 本发明涉及一种用作血管紧张素II受体阻断剂中间体的四唑化合物脱保护方法,提供血管紧张素II受体阻断剂的新型制备方法。 本发明提供由式[3]或[4]表示的化合物或其盐的制备方法,其包括(i)在式(1)或[2]表示的化合物或其盐的存在下,还原式 金属催化剂和碱土金属盐,或(ii)使化合物与特定量的布朗斯台德酸反应:其中每个符号如本说明书中所定义。

    Method for producing biaryl compound

    公开(公告)号:US09624181B2

    公开(公告)日:2017-04-18

    申请号:US14424912

    申请日:2013-08-30

    申请人: API CORPORATION

    发明人: Masahiko Seki

    摘要: The invention provides a production method of a biaryl compound of the formula [3] or a salt thereof, including reacting a 2-phenylazole derivative of the formula [1] or a salt thereof, with a benzene derivative of the formula [2] or a salt thereof in the presence of a metal catalyst, a base, and one or more of (a) a monocarboxylic acid metal salt, (b) a dicarboxylic acid metal salt, (c) a sulfonic acid metal salt, and (d) a phosphate or phosphoric amide metal salt represented by RAxP(O)(OM)y wherein each symbol is as defined herein.

    Deprotection method for tetrazole compound
    4.
    发明授权
    Deprotection method for tetrazole compound 有权
    四唑化合物脱保护方法

    公开(公告)号:US09527821B2

    公开(公告)日:2016-12-27

    申请号:US14429257

    申请日:2013-09-26

    申请人: API CORPORATION

    发明人: Masahiko Seki

    摘要: The present invention relates to a method of deprotecting a tetrazole compound, useful as an intermediate for angiotensin II receptor blockers, and provides a novel production method of angiotensin II receptor blockers.Provided is a production method of a compound represented by the formula [3] or [4] or a salt thereof, including (i) reducing a compound represented by the formula [1] or [2] or a salt thereof in the presence of a metal catalyst and an alkaline earth metal salt, or (ii) reacting the compound with a particular amount of Brønsted acid: wherein each symbol is as defined in the present specification.

    摘要翻译: 本发明涉及一种用作血管紧张素II受体阻断剂中间体的四唑化合物脱保护方法,提供血管紧张素II受体阻断剂的新型制备方法。 本发明提供由式[3]或[4]表示的化合物或其盐的制备方法,其包括(i)在式(1)或[2]表示的化合物或其盐的存在下,还原式 金属催化剂和碱土金属盐,或(ii)使化合物与特定量的布朗斯台德酸反应:其中每个符号如本说明书中所定义。