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filingDate 1985-03-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1986-06-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0157206-A3
titleOfInvention Substituted isochromanes and oxepines, their acid addition salts, medicines containing them and process for their preparation
abstract The invention relates to isochromanes and oxepins of the general formula (I) wherein R¹ is a hydrogen atom or a straight or branched alkyl group with up to 4 carbon atoms, R² is a hydrogen atom or a straight or branched alkyl group having up to 4 C atoms or together with R¹ is an alkylene group having 3 to 5 C atoms, R³ is a hydrogen atom or a straight or branched al yl group with up to 4 C atoms, R⁴ is a hydrogen atom or a straight or branched alkyl group with up to 4 carbon atoms, R⁵ is a hydrogen atom or a straight or branched alkyl group having 1 to 6 carbon atoms or a pyridinyl group, R⁶ is a hydrogen atom, a fluorine, chlorine or bromine atom, a straight or branched alkyl group with 1 to 6 carbon atoms, a hydroxyl or alkoxy group with 1 to 4 carbon atoms or a trifluoromethyl group, R⁷ is a hydrogen atom, a fluorine, chlorine or bromine atom, a straight or branched alkyl group having 1 to 6 C atoms, a hydroxyl or alkoxy group having 1 to 4 C atoms or together with R⁶ a methylenedioxy group, R⁸ is a hydrogen atom, a hydroxyl or alkoxy group with 1 to 4 carbon atoms, m the numbers 1 or 1 and n denotes the numbers 1, 2 or 3, and their acid addition salts.n n n The compounds are calcium antagonistic and antinhypertonic.
priorityDate 1984-03-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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