Toray Industries, Inc.

Mamoru Ishikawa

Hiroshi Nagase

Kiyotaka Ohno

Shintaro Nishio

Kazuhisa Matsumoto

Masaaki Suematsu

Shotaro Matsuoka

Process for producing a nitrile by dehydration reaction of an amide in the presence of a carboxylic acid having the same radical as the amide, or by adding urea to a carboxylic acid with the carboxylic acid either molten or dissolved in a solvent, where the amount of urea used is less than about 0.8 in molar ratio to the carboxylic acid, or when an exhaust gas distillate line connected to the reactor is kept at about 60.degree. C. or higher, or while a gas that is inert to the reaction is fed into the reaction and the produced nitrile and water are concurrently distilled out.

Process for producing a nitrile

Pharmaceutically useful compounds are 5,6,7-trinor-4,8-inter-m-phenylene PGI.sub.2 derivatives such as

5,6,7,-trinor-4,8-inter-m-phenylene 2-nor PGI.sub.2 derivatives and

Pharmaceutically useful compounds are 5,6,7-trinor-4,8-inter-m-phenylene PGI.sub.2 derivatives such as 5,6,7-trinor-4,8-inter-m-phenylene-13,14-didehydro PGI.sub.2, 5,6,7-trinor-4,8-inter-m-phenylene-16,16-dimethyl PGI.sub.2, 5,6,7-trinor-4,8-inter-m-phenylene-17-.alpha.-methyl-20-homo PGI.sub.2, 5,6,7-trinor-4,8-inter-m-phenylene-17,18,19,20-tetranor-16-phenoxy PGI.sub.2, 5,6,7-trinor-4,8-inter-m-phenylene-20-isopropylidene PGI.sub.2, 5,6,7-trinor-4,8-inter-(5-methyl-1,3-phenylene) PGI.sub.2, and 5,6,7-trinor-4,8-inter-m-phenylene-2,3-didehydro-16,17,18,19,20-pentanor-1 5-phenyl PGI.sub.2. They are useful in treatment of ulcers, thrombii and hypertension for example.

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Kamakura, Japan

Mamoru Ishikawa