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公开(公告)号:JPH0513144B2
公开(公告)日:1993-02-19
申请号:JP16401884
申请日:1984-08-03
Applicant: SUMITOMO CHEMICAL CO
Inventor: MINAMII MASAYOSHI , UEDA JUJI
IPC: C07C201/02 , C07C67/00 , C07C201/00 , C07C203/08
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公开(公告)号:JPH04503961A
公开(公告)日:1992-07-16
申请号:JP50296591
申请日:1991-01-10
IPC: C07C201/02 , C07C203/02 , C07C203/04
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公开(公告)号:JPH0244460B2
公开(公告)日:1990-10-04
申请号:JP3618084
申请日:1984-02-29
Applicant: TOA EIYO LTD
Inventor: NARA TAKESHI , HAYASHI HISASHI , SATO KENTARO
IPC: C07C201/02 , C07C67/00 , C07C201/00 , C07C201/16 , C07C203/02 , C07C203/04
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公开(公告)号:JPH0233025B2
公开(公告)日:1990-07-25
申请号:JP5931381
申请日:1981-04-21
Applicant: II AI DEYUHON DE NIMOASU ANDO CO
Inventor: ROBAATO MATSUKOORU
IPC: C07C201/16 , B01J14/00 , B01J19/14 , C07C67/00 , C07C201/00 , C07C201/02 , C07C201/08 , C07C205/06 , C07C205/10 , C07C205/11 , C07C205/12 , C07C209/36
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公开(公告)号:JPS60181052A
公开(公告)日:1985-09-14
申请号:JP3618084
申请日:1984-02-29
Applicant: TOA EIYO LTD
Inventor: NARA TAKESHI , HAYASHI HISASHI , SATOU KENTAROU
IPC: C07C201/02 , C07C67/00 , C07C201/00 , C07C201/16 , C07C203/02 , C07C203/04
Abstract: PURPOSE:To provide the titled composition having high stability and handleability, free from irritation and volatility, and effective as a remedy and preventive for the fit of stenocardia, by compounding isosorbide nitrate with a specific component such as polyvinyl pyrrolidone. CONSTITUTION:Isosorbide nitrate is compounded with one or more components selected from the group of polyvinyl pyrrolidone, methyl-cellulose, hydroxypropylcellulose and hydroxypropylmethylcellulose. The amount of the latter component is 0.2-30pts.wt., especially 1-15pts.wt. per 1pt.wt. of isosorbide nitrate. The composition is prepared preferably by dissolving isosorbide nitrate in a solvent, and then dissolving and/or dispersing the latter component such as polyvinyl pyrrolidone in the solution, however, it may be prepared by mixing the solution or dispersion of isosorbide nitrate with the of the latter component.
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公开(公告)号:JPS60152445A
公开(公告)日:1985-08-10
申请号:JP886884
申请日:1984-01-20
Applicant: TAISHO PHARMA CO LTD
Inventor: NAKAJIMA YOSHIMOTO , OGAWA TOSHIHISA , NAKAZATO ATSUO , KUMAZAWA YUKINARI , SODA KAORU
IPC: C07C203/04 , C07C67/00 , C07C201/00 , C07C201/02
Abstract: PURPOSE:To obtain the titled compound useful as an intermediate of pharmaceuticals, easily, in high purity, without producing hardly separable position isomers, by reducing a lower alkyl ester of 2-nitratopropionic acid with a reducing agent. CONSTITUTION:The objective compound can be produced without producing a position isomer, 2-nitrato-2-propanol, by reducing 2-nitratopropionic acid lower alkyl ester (1-3C alkyl ester) with a borohydride reducing agent (e.g. NaBH4, NaBH4-CaCl2) at 40-70 deg.C, or with aluminum hydride reducing agent (e.g. LiAl H4) in an inert solvent at -50-0 deg.C. The most suitable reducing agent is NaBH4- CaCl2. Since the production of impurity is little, highly purified objective product can be produced easily in high yield.
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公开(公告)号:JPS5896044A
公开(公告)日:1983-06-07
申请号:JP19177281
申请日:1981-12-01
Applicant: MITSUI TOATSU CHEMICALS
Inventor: TAKENAKA SHINJI , NISHIDA TAKESHI , KANEMOTO YOSHIO
IPC: B01J27/00 , C07C67/00 , C07C201/00 , C07C201/02 , C07C201/08 , C07C205/12
Abstract: PURPOSE:To prepare the titled compound useful as an intermediate of dyes, etc., in a short time, in high yield, suppressing the by-production of dinitro compounds, by nitrating chlorobenzene using a nitrating agent comprising a mixture of nitric acid and a concentrated phosphoric acid having specific concentration, at a specific temperature. CONSTITUTION:Mononitrochlorobenzene is prepared in an yield of as high as >=98%, by adding a mixed acid consisting of 98% nitric acid and concentrated phosphoric acid having a concentration of >=72.4wt%, preferably 74-80wt% in terms of P2O5 dropwise to chlorobenzene at 50-120 deg.C, preferably 60-100 deg.C to effect the nitration reaction. The concentrated phosphoric acid can be prepared easily by concentrating ordinary orthophosphoric acid by evaporation, e.g. at 150 deg.C and 20mm.Hg. USE:Intermediate of agricultural chemicals and other industrial chemicals.
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公开(公告)号:JPS5869840A
公开(公告)日:1983-04-26
申请号:JP16675782
申请日:1982-09-27
Applicant: UNION CARBIDE CORP
Inventor: AASAA ROI DOYUMAU JIYUNIA , JIEEMUZU MAIKERU DOUNII , JIYOSEFU PIITAA HENRII , JIYON MARION HAATO
IPC: C07C67/00 , C07C201/00 , C07C201/02 , C07C201/04 , C07C203/00 , F16L59/14
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公开(公告)号:WO2012089769A1
公开(公告)日:2012-07-05
申请号:PCT/EP2011/074152
申请日:2011-12-28
Applicant: PROCOS S.P.A. , BAROZZA, Alessandro , COLOMBO, Matteo , ROLETTO, Jacopo , PAISSONI, Paolo
Inventor: BAROZZA, Alessandro , COLOMBO, Matteo , ROLETTO, Jacopo , PAISSONI, Paolo
IPC: C07C201/02
CPC classification number: C07C201/02 , C07C203/04
Abstract: Disclosed is a process for the synthesis of Nicorandil (1), 2-(nicotinamide)ethyl nitrate, starting from N-(2-hydroxyethyl)nicotinamide (15), using nitration with nitric acid in the presence of acetic anhydride Said synthesis method is particularly advantageous because it solves the safety problems involved in the use of nitric acid as nitrating agent, and allows a product with excellent yields and quality to be isolated.
Abstract translation: 公开了一种从N-(2-羟乙基)烟酰胺(15)开始合成尼可地尔(1),2-(烟酰胺)乙酸乙酯的方法,使用硝酸在乙酸酐存在下硝化所述合成方法为 特别有利,因为它解决了使用硝酸作为硝化剂所涉及的安全问题,并且能够分离出优异的产率和质量的产品。
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公开(公告)号:WO2009149053A3
公开(公告)日:2010-05-14
申请号:PCT/US2009045920
申请日:2009-06-02
Applicant: REDDYS LAB LTD DR , REDDYS LAB INC DR , KOLLA NAVEEN KUMAR , GANGULA SRINIVAS , NAREDLA ANITHA , BADDAM SUDHAKAR REDDY , PATIL SUMEET VISHWASRAO , SIGALA ASHOK , CHITTAPATHINA RAGHUNATH BABU VENKATA , MEDISETTI RAMA KRISHNA VENKATA , MANUDHANE KUSHAL SURAJMAL , NARRA SANTOSH REDDY , KOTAGIRI VIJAYA KUMAR
Inventor: KOLLA NAVEEN KUMAR , GANGULA SRINIVAS , NAREDLA ANITHA , BADDAM SUDHAKAR REDDY , PATIL SUMEET VISHWASRAO , SIGALA ASHOK , CHITTAPATHINA RAGHUNATH BABU VENKATA , MEDISETTI RAMA KRISHNA VENKATA , MANUDHANE KUSHAL SURAJMAL , NARRA SANTOSH REDDY , KOTAGIRI VIJAYA KUMAR
IPC: C07C201/02 , A61K31/21 , C07C203/04
CPC classification number: C07C201/02 , C07B2200/13 , C07C69/734 , C07C203/04
Abstract: Processes for the preparation of naproxcinod and its purification, solid dispersions of naproxcinod with a pharmaceutically acceptable carrier, and processes for making dispersions. Also provided is crystalline 2-(S)-(4-chlorobutyl)-2-(6-methoxy-2-naphthyl)-propanoate and methods for its preparation.
Abstract translation: 用于制备萘普生和其纯化的方法,萘普生与药学上可接受的载体的固体分散体,以及制备分散体的方法。 还提供了2-(S) - (4-氯丁基)-2-(6-甲氧基-2-萘基) - 丙酸酯的结晶及其制备方法。
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