Details for Patent: 4,731,374

Title:	Tetrahydro-benzthiazoles, the preparation thereof and their use as intermediate products or as pharmaceuticals
Abstract:	This invention relates to new tetrahydrobenzthiazoles of general formula ##STR1## wherein R.sub.1 represents a hydrogen atom, an alkyl group, an alkenyl or alkynylk group, an alkanoyl group, a phenyl alkyl or phenyl alkanoyl group, while the above mentioned phenyl nuclei may each be substituted by 1 or 2 halogen atoms, R.sub.2 represents a hydrogen atom or an alkyl group, R.sub.3 represents a hydrogen atom, an alkyl group a cycloalkyl group, an alkenyl or alkynyl group, an alkanoyl group, a phenyl alkyl or phenyl alkanoyl group, while the phenyl nucleus may be substituted by flurorine, chlorine or bromine atoms, R.sub.4 represents a hydrogen atom, an alkyl group, an alkyl or alkenyl group, or R.sub.3 and R.sub.4 together with the nitrogen atom between them represent a pyrrolidino, piperidino, hexamethyleneimino or morpholino group, the enantiomers and the acid addition salts thereof. The compounds of general formula I above in which one of the groups R.sub.1 or R.sub.3 or both groups R.sub.1 and R.sub.3 represent an acyl group are valuable intermediate products for preparing the other compounds of general formula I which have valuable pharmacological properties. The new compounds may be prepared using methods known per se.
Inventor(s):	Griss, deceased; Gerhart (late of Biberach, DE), Hurnaus; Rudolf (Biberach, DE), Kobinger; Walter (Vienna, AT), Pichler; Ludwig (Vienna, AT), Bauer; Rudolf (Wiesbaden, DE), Mierau; Joachim (Mainz, DE), Hinzen; Dieter (Zornheim, DE), Schingnitz; Gunter (Kreuznach, DE)
Assignee:	Dr. Karl Thomae GmbH (Biberach an der Riss, DE)
Filing Date:	Dec 19, 1985
Application Number:	06/810,947
Claims:	1. A tetrahydro-benzthiazole of the formula: ##STR15## wherein R.sub.1 is a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, an alkenyl or alkynyl group each having 3 to 6 carbon atoms, an alkanoyl group having 1 to 6 carbon atoms, a phenyl alkyl or phenyl alkanoyl group having 1 to 3 carbon atoms in the alkyl part, wherein the above mentioned phenyl nuclei may be substituted by 1 or 2 halogen atoms; R.sub.2 is a hydrogen atom or an alkyl group with 1 to 4 carbon atoms; and R.sub.3 and R.sub.4 together with the nitrogen atom between them form a pyrrolidino group; or, a pharmaceutically acceptable acid addition salt thereof. 2. A tetrahydro-benzthiazole of formula I, as claimed in claim 1, wherein the ##STR16## group is in the 5 or 6-position. 3. A tetrahydro-benzthiazole of the formula: ##STR17## wherein R.sub.1 is a hydrogen atom, an alkyl group having 1 to 3 carbon atoms, an allyl, benzyl, 2-chloro-benzyl, 4-chloro-benzyl, 3,4-dichloro-benzyl or phenylethyl group; R.sub.2 is a hydrogen atom, a methyl or ethyl group; and R.sub.3 and R.sub.4 together with the nitrogen atom between them form a pyrrolidino group, wherein said pyrrolidino group is in the 5- or 6-position; or, a pharmaceutically acceptable acid addition salt thereof. 4. A tetrahydro-benzthiazole of formula Ia, as claimed in claim 3, wherein the ##STR18## group is in the 6-position. 5. A tetrahydro-benzthiazole of the formula: ##STR19## wherein R.sub.1 and R.sub.2 together with the nitrogen atom between them form an amino or allylamino group; and, R.sub.3 and R.sub.4 together with the nitrogen atom between them form a pyrrolidino group. 6. 2-amino-6-pyrrolidino-4,5,6,7-tetrahydro-benzthiazole, or a pharmaceutically acceptable acid addition salt thereof. 7. A pharmaceutical composition for treating parkinsonism or Parkinson's Disease comprising a therapeutically effective amount of a compound of claims 3, 4, 5 or 6 and a pharmaceutically acceptable carrier. 8. A method of treating parkinsonism which comprises administering to a host suffering from same a therapeutically effective amount of a compound of claims 3, 4, 5 or 6. 9. A method of treating Parkinson's disease which comprises administering to a host suffering from same a therapeutically effective amount of a compound of claims 3, 4, 5 or 6.