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filingDate 1984-03-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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publicationDate 1984-09-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0118848-A2
titleOfInvention Ergoline derivatives, process for their preparation and their pharmaceutical application
abstract R Wasserstoff und NR' R", wobei R' R" für O 2 , H 2' C 1-4 -Dialkyl oder gemeinsam einen 3- bis 9-gliedrigen Ring bildet oder R' und R" jeweils allein für Wasserstoff, C 1-4 -Alkyl und C 1-10 -Acyl, R' für Wasserstoff, C 1-4 -Alkyl, C 1-10 -Acyl, C 6-8 -Aryl- und C 1-4 -Alkylsulfonyl, R 2 für Wasserstoff oder Halogen, wenn C 2 = C 3 eine C=C-Doppelbindung, oder Wasserstoff, wenn C 2 = C 3 eine CC-Einfachbindung darstellt, für C 1-4 -Alkyl stehen. Diese Verbindungen werden nach an sich bekannten Verfahren hergestellt. Sie zeigen eine ausgeprägte Wirkung auf das Zentralnervensystem und sind z.B. als Antidepressiva, Neuroleptika oder Antihypertensiva geeignet. Substituted ergolines of the general formula and their acid addition salts, in which the 8-position urea side chain can be a- or β-position, C 2 = C 3 and Cg = C 10 denote a CC single or C = C double bond and R is hydrogen and NR 'R ", where R'R" for O 2 , H 2 ' C 1-4 dialkyl or together forms a 3- to 9-membered ring or R' and R "each alone for hydrogen, C 1 -4 alkyl and C 1-10 acyl, R 'is hydrogen, C 1-4 alkyl, C 1-10 acyl, C 6-8 aryl and C 1-4 alkylsulfonyl, R 2 is hydrogen or halogen if C 2 = C 3 is a C = C double bond, or hydrogen if C 2 = C 3 is a CC single bond, represent C 1-4 alkyl. These compounds are produced by methods known per se. They have a pronounced effect on the central nervous system and are suitable, for example, as antidepressants, neuroleptics or antihypertensives.
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