Manufacture of trialkyltrithiophosphites and trialkylphosphorothioates
    1.
    发明授权
    Manufacture of trialkyltrithiophosphites and trialkylphosphorothioates 失效
    三烷基三硫代亚磷酸酯和三烷基硫代磷酸酯的制备

    公开(公告)号:US3885002A

    公开(公告)日:1975-05-20

    申请号:US35561473

    申请日:1973-04-30

    发明人: BARBER F TAYLOR

    IPC分类号: C07F9/17 C07F9/202 C07F9/16

    CPC分类号: C07F9/17 C07F9/202

    摘要: The manufacture of trialkyltrithiophosphites by reacting an excess of an alkyl mercaptan with phosphorous trihalide and scrubbing of noncondensible reactor off-gases with strong caustic solution, continuing the scrubbing until the strong caustic solution becomes spent though still mildly alkaline when the alkyl mercaptan separates into a separate phase. The mercaptans are separated to recycle. The trialkyltrithiophosphite can be oxidized to trialkyltriphosphorothioate with further stripping and recovery of remaining mercaptans.

    摘要翻译: 通过使过量的烷基硫醇与三卤化磷反应并用强碱性溶液洗涤不可冷凝的反应器废气来制造三烷基三硫代亚磷酸酯,当烷基硫醇分离成单独的时,继续进行洗涤,直到强碱性溶液消耗,但仍然是弱碱性的 相。 硫醇分离回收。 三烷基三亚磷酸酯可以被氧化成三烷基三硫代磷酸酯,进一步剥离和回收剩余的硫醇。

    Acyclic Thiol Prodrugs
    4.
    发明公开

    公开(公告)号:US20230212200A1

    公开(公告)日:2023-07-06

    申请号:US18147172

    申请日:2022-12-28

    IPC分类号: C07F9/202 C07F9/203

    CPC分类号: C07F9/202 C07F9/203

    摘要: Disclosed herein are acyclic thiol prodrugs, and pharmaceutical compositions thereof. The prodrugs and pharmaceutical compositions thereof may be used to treat or prevent medical disorders such as, for example cystinosis, cystinuria, cancer neurodegenerative disease, Parkinson's disease, Huntington's disease, malaria, nonalcoholic fatty liver disease, radiation poisoning, arsenic poisoning, radioprotection, Wilson's disease or rheumatoid arthritis.

    Echothiophate iodide process
    7.
    发明授权

    公开(公告)号:US09708352B2

    公开(公告)日:2017-07-18

    申请号:US15108790

    申请日:2015-01-01

    IPC分类号: C07F9/202 C07F9/17

    摘要: The present invention relates to a process for preparation of Echothiophate Iodide (I). Echothiophate Iodide (I) obtained by the process of the present invention is obtained as new crystalline form designated as Form-SET. The process for preparation of Echothiophate Iodide (I) according to present invention is an ecofriendly process that avoids the use of hazardous solvent systems and provides Echothiophate Iodide (I) of high purity. Pharmaceutical composition of the said crystalline Form-SET of Echothiophate Iodide (I) of high purity is useful in the treatment of ocular disorders like Glaucoma.

    Preparation of trialkyl trithiophosphites
    8.
    发明授权
    Preparation of trialkyl trithiophosphites 失效
    三烷基三硫代亚磷酸酯的制备

    公开(公告)号:US3922325A

    公开(公告)日:1975-11-25

    申请号:US37224173

    申请日:1973-06-21

    发明人: ANDERSON JOHN E

    IPC分类号: C07F9/202

    CPC分类号: C07F9/202

    摘要: In the preparation of trialkyl trithiophosphites by the reaction of phosphorus trihalide with alkyl mercaptan, the addition of a few parts per million of water increases the reaction rate and ultimate yield of desired trialkyl trithiophosphite.

    摘要翻译: 在通过三卤化磷与烷基硫醇的反应制备三烷基三硫代亚磷酸酯时,每百万分之一份水中的添加增加了所需三烷基三硫代亚磷酸酯的反应速率和最终产率。

    Process for the preparation of dimethyl-thiophosphite or of organothiophosphonous acid o-monomethyl ester
    9.
    发明授权
    Process for the preparation of dimethyl-thiophosphite or of organothiophosphonous acid o-monomethyl ester 失效
    制备二甲基 - 硫代磷酸酯或有机酸性磷酸二甲酯的方法

    公开(公告)号:US3655835A

    公开(公告)日:1972-04-11

    申请号:US3655835D

    申请日:1969-05-05

    申请人: BAYER AG

    发明人: SCHLIEBS REINHARD

    IPC分类号: C07F9/202 C07F9/48 C07F9/16

    CPC分类号: C07F9/202 C07F9/48

    摘要: REACTING TRIMETHYLPOSPHITE OR ORGANO-PHOSPHONOUS ACID O,O-DIMETHYL ESTER WITH HYDROGEN SULFIDE IN THE PRESENCE OF A WEAK ORGANIC BASE (THE PKA OF WHICH IN AQUEOUS SOLUTION IS ABOT 0.5-8) AT A TEMPERATURE OF SUBSTANTIALLY BETWEEN ABOUT 0-70*C. AND A STARTING PRESSURE OF SUBSTANTIALLY BETWEEN ABOUT 1-65 ATMOSPHERES ABSOLUTE, TO FORM IN HIGH YIELD AND PURITY THE CORRESPONDING KNOWN DIMETHYL-THIOPHOSPHITE OR ORGANO-THIOPHOSPHONOUS ACIDO-MONO METHYL ESTER, WHICH ARE KNOWN INTERMEDIATES USEABLE FOR THE SYNTHESIS OF KNOWN BIOCIDAL, ESPECIALLY INSECTICIDAL, PHOSPHORIC ACID ESTERS.