| abstract |
New substituted thienobenzodiazepinones of the general formula are described wherein R is a hydrogen atom or a lower alkyl radical, R 2 is a halogen atom, a hydrogen atom or a lower alkyl radical, X is an oxygen atom or the groups -NH- or -NCH 3 and R is 1-methyl-4-piperidinyl-, 4-methyl Mean -1-piperazinyl or 3a- or 3ß-tropanyl and their acid addition salts, medicaments containing these compounds and processes for the preparation of these compounds. The compounds of the general formula show a very good antiulcerogenic and gastric acid secretion-inhibiting effect, undesirable side effects being largely reduced. |