PROCESS FOR THE SYNTHESIS OF 2-BENZHYDRYL-3 QUINUCLIDINONE

    公开(公告)号:US20200339561A1

    公开(公告)日:2020-10-29

    申请号:US16760324

    申请日:2018-10-30

    Applicant: Procos S.P.A.

    Abstract: The present invention discloses a process for the preparation of 2-benzhydryl-3-quinuclidinone (1). (I). The process of the invention allows to obtain the intermediate 2-benzhydryl-3-quinuclidinone (1) by reaction of 2-benzylidene-3-quinuclidinone (2) with the Grignard reagent phenyl-magnesium halide, in particular chloride or bromide, in the presence of catalytic amounts of copper (I) salts. Taking advantage of the high efficiency of the catalytic system of the copper (I) salts, 2-benzhydryl-3-quinuclidinone (1) is obtained in higher yields than those of the known processes. Advantageously, since the amounts of copper (I) salts are catalytic, the latter can easily be removed from the reaction mixture, and the process is carried out in the presence of solvents less toxic and expensive than those used in the state of the art.

    PROCESS FOR THE SYNTHESIS OF CHLORZOXAZONE
    12.
    发明申请
    PROCESS FOR THE SYNTHESIS OF CHLORZOXAZONE 有权
    合成氯罗沙星的方法

    公开(公告)号:US20170022172A1

    公开(公告)日:2017-01-26

    申请号:US15214499

    申请日:2016-07-20

    Applicant: Procos S.P.A.

    CPC classification number: C07D263/58

    Abstract: Disclosed is a process for the synthesis of chlorzoxazone (1) from 4-chloro-2-aminophenol and ethyl chloroformate in the presence of a base. The process is particularly advantageous because it uses ethyl chloroformate instead of triphosgene, a highly dangerous reagent that releases phosgene and must be handled with extremely strict procedures to guarantee the safety of operators in industrial facilities.Ethyl chloroformate allows the possibility of working with a number of solvents, including water.The yield and purity of the product obtained are very high.

    Abstract translation: 获得的产物的产率和纯度非常高。

    Process for the industrial synthesis of lurasidone
    13.
    发明授权
    Process for the industrial synthesis of lurasidone 有权
    卢拉西酮工业化合物工艺

    公开(公告)号:US09518047B2

    公开(公告)日:2016-12-13

    申请号:US15028962

    申请日:2014-10-16

    Applicant: PROCOS S.P.A.

    CPC classification number: C07D417/12

    Abstract: Disclosed is a process for the industrial synthesis of Lurasidone from (1R,2R)-cyclohexane-1,2-diyldimethanol (1), 3-(piperazin-1-yl)benzo[d]isothiazole (3) and (3aR,4R,7R,7aS)-3a,4,7,7a-tetrahydro-4,7-methanoisobenzofuran-1,3-dione (6).). Said process is optimised to obtain Lurasidone with high yields and high purities by preparing highly pure synthesis intermediates, using critical raw materials and reagents in amounts close to the stoichiometric amounts, increasing productivity and reducing the costs and environmental impact of the process.

    Process for the synthesis of pirfenidone

    公开(公告)号:US10472325B2

    公开(公告)日:2019-11-12

    申请号:US15771050

    申请日:2016-10-27

    Applicant: PROCOS S.p.A.

    Abstract: Disclosed is a process for the synthesis of Pirfenidone (1) from 5-methyl-2(1H)-pyridinone and chlorobenzene in the presence of a catalytic system consisting of a copper salt and an organic ligand, in the presence of a base. The process exploits the high efficiency of the catalytic system consisting of copper(I) salt and an organic ligand in the presence of an inorganic base in the N-amidation reaction of chlorobenzene, a cheap reagent also usable as solvent in this case; reaction conditions at high temperatures, at atmosphere pressure or higher, produce a reaction with good yields.

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