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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.
Inventor: Monica Donnola , Matteo Mossotti , Mauro Barbero , Jacopo Roletto , Paolo Paissoni
IPC: C07D453/02
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.
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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.
Inventor: Luigi Bogogna , Lavinia Cicione , Alessandro Barozza , Jacopo Roletto , Paolo Paissoni
IPC: C07D263/58
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。
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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.
Inventor: Tommaso Angelini , Piergiorgio Bettoni , Jacopo Roletto , Paolo Paissoni
IPC: C07D417/12
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.
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公开(公告)号:US11939342B2
公开(公告)日:2024-03-26
申请号:US17426356
申请日:2020-03-25
Applicant: PROCOS S.P.A.
Inventor: Alberto Lena , Antonio Toppino , Katia Miele , Jacopo Roletto , Paolo Paissoni
IPC: C07D498/22
CPC classification number: C07D498/22
Abstract: A process for the preparation of midostaurin with high purity, particularly a process for the preparation of midostaurin with a content of oxidation impurities lower than 0.1% comprising the treatment of crude midostaurin or staurosporine with strong organic or inorganic acids in a water-immiscible solvent and, optionally, also with reducing silanes is described.
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公开(公告)号:US20220194977A1
公开(公告)日:2022-06-23
申请号:US17594455
申请日:2020-04-23
Applicant: PROCOS S.P.A.
Inventor: Fabio Morana , Jacopo Roletto , Paolo Paissoni
IPC: C07H15/14
Abstract: The present invention relates to a new process for preparing Sugammadex.
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公开(公告)号:US11344550B2
公开(公告)日:2022-05-31
申请号:US16760685
申请日:2018-10-23
Applicant: Procos S.P.A.
Inventor: Fabio Morana , Stefano Gobbato , Lucia Cozzi , Jacopo Roletto , Paolo Paissoni
IPC: C07D403/06 , A61K31/513
Abstract: The present invention concerns a process for the preparation of the crystalline form III of Tipiracil hydrochloride having a content of residual solvents lower than the ICH limits. Said process is advantageous with respect to the known processes because it allows the production of the form III of Tipiracil hydrochloride suitable for use in the preparation of pharmaceutical finished products.
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公开(公告)号:US20200330465A1
公开(公告)日:2020-10-22
申请号:US16760685
申请日:2018-10-23
Applicant: Procos S.P.A.
Inventor: Fabio Morana , Stefano Gobbato , Lucia Cozzi , Jacopo Roletto , Paolo Paissoni
IPC: A61K31/513
Abstract: The present invention concerns a process for the preparation of the crystalline form III of Tipiracil hydrochloride having a content of residual solvents lower than the ICH limits. Said process is advantageous with respect to the known processes because it allows the production of the form III of Tipiracil hydrochloride suitable for use in the preparation of pharmaceutical finished products.
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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.
Inventor: Matteo Mossotti , Alessandro Barozza , Jacopo Roletto , Paolo Paissoni
IPC: C07D213/64
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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