Intermediates for the preparation of pyrazoloazole photographic
couplers, processes of making and adjusting them
    1.
    发明授权
    Intermediates for the preparation of pyrazoloazole photographic couplers, processes of making and adjusting them 失效
    用于制备吡唑并咪唑摄影成色剂的中间体,制备和调整它们的过程

    公开(公告)号:US5981760A

    公开(公告)日:1999-11-09

    申请号:US789511

    申请日:1997-01-27

    IPC分类号: G03C7/38 C07D487/04 C09B57/00

    CPC分类号: C07D487/04

    摘要: There are described intermediates for the preparation of known pyrazoloazole photographic magenta dye forming couplers and processes for making and using these intermediates. The intermediates are low molecular weight compounds represented by the structure: ##STR1## wherein: R, X, R.sup.1 and Y are defined herein. The process for making these intermediates involves diazotizing a 5-amino-1H-pyrazole to produce a 5-diazo-1H-pyrazole, then condensing the diazotized product with an active methine or methylene compound having a pKa of 14 or less to produce a substituted hydrazone and then subjecting the hydrazone to cyclization and reduction, in either order.

    摘要翻译: 描述了制备已知的吡唑并唑摄影品红染料形成成色剂的中间体和制备和使用这些中间体的方法。 中间体是由以下结构表示的低分子量化合物:其中:R,X,R 1和Y如本文所定义。 制备这些中间体的方法包括将5-氨基-1H-吡唑重氮化以制备5-重氮-1H-吡唑,然后将重氮化产物与pKa为14或更小的活性次甲基或亚甲基化合物缩合,生成取代的 腙,然后以任一顺序对腙进行环化和还原。

    Intermediates for the preparation of pyrazoloazole photographic
couplers, processes of making and using them
    4.
    发明授权
    Intermediates for the preparation of pyrazoloazole photographic couplers, processes of making and using them 失效
    制备吡唑并咪唑摄影成色剂的中间体,制备和使用它们的过程

    公开(公告)号:US5457210A

    公开(公告)日:1995-10-10

    申请号:US231602

    申请日:1994-04-22

    IPC分类号: G03C7/38 C07D487/04 C09B57/00

    CPC分类号: C07D487/04

    摘要: There are described intermediates for the preparation of known pyrazoloazole photographic magenta dye forming couplers and processes for making and using these intermediates. The intermediates are low molecular weight compounds represented by the structure: ##STR1## wherein: R, X, R.sup.1 and Y are defined herein.The process for making these intermediates involves diazotizing a 5-amino-1H-pyrazole to produce a 5-diazo-1H-pyrazole, then condensing the diazotized product with an active methine or methylene compound having a pKa of 14 or less to produce a substituted hydrazone and then subjecting the hydrazone to cyclization and reduction, in either order.

    摘要翻译: 描述了制备已知的吡唑并唑摄影品红染料形成成色剂的中间体和制备和使用这些中间体的方法。 中间体是由以下结构表示的低分子量化合物:其中:R,X,R 1和Y如本文所定义。 制备这些中间体的方法包括将5-氨基-1H-吡唑重氮化以制备5-重氮-1H-吡唑,然后将重氮化产物与pKa为14或更小的活性次甲基或亚甲基化合物缩合,生成取代的 腙,然后以任一顺序对腙进行环化和还原。

    Oxidative desulfurization and halogenation of thioacylated
pyrazolotriazole compounds
    5.
    发明授权
    Oxidative desulfurization and halogenation of thioacylated pyrazolotriazole compounds 失效
    硫代酰化吡唑并三唑化合物的氧化脱硫和卤化

    公开(公告)号:US5461164A

    公开(公告)日:1995-10-24

    申请号:US213786

    申请日:1994-03-14

    IPC分类号: G03C7/30 C07D487/04

    CPC分类号: C07D487/04

    摘要: A process for the desulfurization, and halogenation of a 1-acyl-7-acylthio-3,6-disubstituted-1H-pyrazolo[5,1-c]-1,2,4-triazole first compound comprises reacting the compound with an excess of a halogenating agent whereby a 3,6-disubstituted-7,7-dihalo-1H-pyrazolo[5,1-c]-1,2,4-triazole compound is formed.

    摘要翻译: 1-酰基-7-酰基硫代-3,6-二取代-1H-吡唑并[5,1-c] -1,2,4-三唑第一化合物的脱硫和卤化的方法包括使化合物与 过量的卤化剂,由此形成3,6-二取代-7,7-二卤代-1H-吡唑并[5,1-c] -1,2,4-三唑化合物。

    Process for preparation of a
4-amino-5-mercapto-3-substituted-�1,2,4!triazole compound
    6.
    发明授权
    Process for preparation of a 4-amino-5-mercapto-3-substituted-�1,2,4!triazole compound 失效
    制备4-氨基-5-巯基-3-取代的 - [1,2,4]三唑化合物的方法

    公开(公告)号:US5864042A

    公开(公告)日:1999-01-26

    申请号:US10009

    申请日:1998-01-21

    IPC分类号: C07D249/12

    CPC分类号: C07D249/12

    摘要: The invention provides a process for preparing a 4-amino-5-mercapto-3-substituted-�1,2,4!triazole comprising reacting a thiocarbohydrazide with a carboxylic acid in the presence of an organic solvent and a boron compound having the formula ##STR1## where R.sup.2, R.sup.3, and R.sup.4 are independently selected from the group consisting of hydrogen, hydroxy, amino, alkyl, aryl, alkoxy, and aryloxy groups. The process provides a safer low temperature process for preparing the desired compound.

    摘要翻译: 本发明提供了一种制备4-氨基-5-巯基-3-取代的 - [1,2,4]三唑的方法,包括在有机溶剂和具有下式的硼化合物存在下,使硫代碳酰肼与羧酸反应: 其中R 2,R 3和R 4独立地选自氢,羟基,氨基,烷基,芳基,烷氧基和芳氧基。 该方法提供了用于制备所需化合物的更安全的低温方法。