Substituted pyrido (1,2-c)imidazo(1,2-a)benzimidazoles, processe

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...

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546 64, 546278, 546296, A61K 3144, C07D47112

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active

045857750

ABSTRACT:
The invention relates to compounds of the formula ##STR1## in which R.sup.1 and R.sup.2 are identical or different and are hydrogen, alkyl, trifluoromethyl, halogen, alkoxycarbonyl, alkoxy or alkanoyl, R.sup.3, R.sup.4 and R.sup.5 are identical or different and are hydrogen, methyl, alkoxy or alkoxyethoxy, and R is hydrogen or a group SR.sup.6, in which R.sup.6 is the lone, unpaired electron of the 12-sulfenyl radical, hydrogen, optionally substituted alkyl, alkenyl, alkynyl, alkanoyl, optionally mono- or poly-substituted benzoyl, fuoryl, phenacyl, phenoxyacetyl, phenylacetyl or another conventional thiol-protective group, and to physiologically acceptable salts thereof, and to processes for their preparation, to their use as a gastric acid secretion inhibitor and to pharmaceutical preparations based on these compounds.

REFERENCES:
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patent: 3880870 (1975-04-01), Ledig et al.
patent: 3911130 (1975-10-01), Herbst et al.
patent: 4254127 (1981-03-01), Vandenberk et al.
patent: 4255573 (1981-03-01), Adhikary
patent: 4472409 (1984-09-01), Senn-Bilfinger
Irikura et al., Chemical Abstracts, vol. 78, 4251r, 1973.
Brimblecombe et al., Proceedings of the B.P.S., 1/8/75-1/10/75, pp. 435P-436P.

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