OUCHI SHINKO CHEMICAL INDUSTRIAL CO., LTD. (Japan)
Inventor
Aoyagi Shigenobu
Yamada Ryo
Abstract
The present disclosure provides a novel synthetic intermediate of prostaglandin or an optically active substance thereof, and a production method that uses the same. More specifically, in the method according to the present disclosure for producing prostaglandin or an optically active substance thereof, a compound represented by any of general formulas (I) through (IV) or an optically active substance thereof is used as the synthetic intermediate.
C07C 317/18 - SulfonesSulfoxides having sulfone or sulfoxide groups and singly-bound oxygen atoms bound to the same carbon skeleton with sulfone or sulfoxide groups bound to acyclic carbon atoms of the carbon skeleton
C07C 45/64 - Preparation of compounds having C=O groups bound only to carbon or hydrogen atomsPreparation of chelates of such compounds by reactions not involving the formation of C=O groups by introduction of functional groups containing oxygen only in singly bound form
C07C 49/707 - Unsaturated compounds containing a keto group being part of a ring containing hydroxy groups a keto group being part of a three- to five-membered ring
C07C 67/14 - Preparation of carboxylic acid esters from carboxylic acid halides
C07C 69/63 - Halogen-containing esters of saturated acids
C07C 315/04 - Preparation of sulfonesPreparation of sulfoxides by reactions not involving the formation of sulfone or sulfoxide groups
C07C 405/00 - Compounds containing a five-membered ring having two side-chains in ortho position to each other, and having oxygen atoms directly attached to the ring in ortho position to one of the side-chains, one side-chain containing, not directly attached to the ring, a carbon atom having three bonds to hetero atoms with at the most one bond to halogen, and the other side-chain having oxygen atoms attached in gamma-position to the ring, e.g. prostaglandins
OUCHI SHINKO CHEMICAL INDUSTRIAL CO., LTD. (Japan)
Inventor
Aoyagi Shigenobu
Yamada Ryo
Abstract
The present disclosure provides: a novel synthesis intermediate for beraprost or an optically active form thereof; and a production method using the synthesis intermediate. More specifically, in the present disclosure, a compound represented by general formula (I) or (II) or an optically active form thereof is used as a synthesis intermediate in the production of beraprost or an optically active form thereof.
C07D 307/93 - Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems condensed with a ring other than six-membered
A61K 31/343 - Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide condensed with a carbocyclic ring, e.g. coumaran, bufuralol, befunolol, clobenfurol, amiodarone
A61P 11/00 - Drugs for disorders of the respiratory system
C07F 7/18 - Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
Ouchi Shinko Chemical Industrial Co., Ltd. (Japan)
Inventor
Kasai, Hitoshi
Koseki, Yoshitaka
Kamishima, Takaaki
Aoyagi, Shigenobu
Abstract
The present invention provides: industrially desirable and novel optically-active cyclopentenone derivatives; and a novel industrial manufacturing method. The novel optically-active cyclopentenone derivatives and method for manufacturing the same are, respectively: an intermediate for industrially desirable and novel prostaglandin derivatives and the like; and a method for manufacturing the same. It is expected that the present invention will be commercialized and industrialized.
C07F 7/18 - Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
C07B 51/00 - Introduction of protecting groups or activating groups, not provided for in groups
C07B 63/02 - PurificationSeparation specially adapted for the purpose of recovering organic compoundsStabilisationUse of additives by treatment giving rise to a chemical modification
C12P 7/38 - Cyclopentanone- or cyclopentadione- containing products
OUCHI SHINKO CHEMICAL INDUSTRIAL CO., LTD. (Japan)
Inventor
Kasai Hitoshi
Koseki Yoshitaka
Kamishima Takaaki
Aoyagi Shigenobu
Abstract
The present invention provides: industrially desirable and novel optically-active cyclopentenone derivatives; and a novel industrial manufacturing method. The novel optically-active cyclopentenone derivatives and method for manufacturing the same are, respectively: an intermediate for industrially desirable and novel prostaglandin derivatives and the like; and a method for manufacturing the same. It is expected that the present invention will be commercialized and industrialized.
Ouchi Shinko Chemical Industrial Co., Ltd. (Japan)
Inventor
Akimoto, Keiichi
Ariga, Nozomi
Okawa, Kyouji
Komatsu, Tomoyuki
Shibuya, Hiroshi
Abstract
A sulfenamide vulcanization accelerator is provided that acts satisfactorily slowly on a vulcanization reaction, produces no carcinogenic nitrosamine, and is free from environmental hygiene problems such as bioaccumulation. Also provided is an N-alkyl-N-t-butylbenzothiazole-2-sulfenamide represented by formula [I]. The vulcanization accelerator is a vulcanization accelerator for rubber, containing this compound. Furthermore provided is a process for producing the vulcanization accelerator.
wherein R represents methyl, ethyl, n-propyl, or n-butyl.
OUCHI SHINKO CHEMICAL INDUSTRIAL CO., LTD. (Japan)
Inventor
Akimoto, Keiichi
Ariga, Nozomi
Okawa, Kyouji
Komatsu, Tomoyuki
Shibuya, Hiroshi
Abstract
A sulfonamide-based vulcanization accelerator is provided which acts sufficiently slowly on a vulcanization reaction, generates no carcinogenic nitrosamine, and is free from hygienic or environmental problems such as bioaccumulation. Also provided is an N-alkyl-N-t-butylbenzothiazole-2-sulfenamide represented by formula (I). The vulcanization accelerator for rubbers contains this compound. Furthermore provided is a process for producing the same. [Chemical formula 1] [R represents methyl, ethyl, n-propyl, or n-butyl.]