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filingDate 1994-01-13^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c01afac73cca356c25ec33b4aec20858
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7d788d19248262366503d03886d252ab
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f67a5781dfe48dfdad887a78c983d418
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_87c2684ca9223e97b4970ebc98ed2dfe
publicationDate 1995-01-13^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H0710855-A
titleOfInvention Process for producing perhydro-1,4-thiazepine derivative
abstract (57) [Summary] [Structure] General formula (In the formula, R 1 : an alkyl group, a cycloalkylalkyl group, an aralkyl group; R 2 : a protecting group for a carboxy group; R 4 , R 5 : H, a heterocyclic group; provided that R 4 and R 5 are simultaneously H Not shown. A compound having the general formula XCH 2 CO 2 R 6 (wherein X is a halogen atom; R 6 is a protecting group for a carboxy group) is condensed in the presence of a base to give a compound of the general formula (Wherein R 1 , R 2 , R 4 , R 5 , R 6 are as defined above), and the protecting group R 6 for the carboxy group of this compound is removed. , General formula: A method for producing a perhydro-1,4-thiazepine derivative having the formula (wherein R 1 , R 2 , R 4 , and R 5 are as defined above). [Effect] This compound has an angiotensin converting enzyme inhibitory action and is useful as an antihypertensive drug.
priorityDate 1994-01-13^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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