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filingDate 1996-11-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4d0d15d73bfb45e4b8e25d5967a29ef0
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publicationDate 1997-06-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0778264-A1
titleOfInvention Tertiary amines having antimycotic and cholesterol lowering activity
abstract A 1 Alkyl oder Alkenyl und A 2 Cycloalkyl, Cycloalkyl-alkyl oder eine gegebenenfalls substituierte Alkyl- oder Alkenylgruppe und, falls A 1 Alkyl ist, A 2 auch OH sein kann, A 3 und A 4 Wasserstoff oder Alkyl sind oder A 1 zusammen mit A 2 oder mit A 3 eine gegebenenfalls substituierte Alkylen-, Alkenylen- oder Alkadienylengruppe A 1 -A 2 bzw. A 1 -A 3 bildet, nwobei in einer Gruppe A 1 -A 2 oder A 1 -A 3 bis zu 2 C-Atome durch ein (oder zwei) N-Atom(e) und/oder durch eine Gruppe N-Alkyl ersetzt sein können, p = 1 und L Phenylen oder direkt oder über O, NH oder N(Alkyl oder Alkanoyl) an M gebundenes Alkylen oder Alkenylen mit insgesamt bis zu 11 C-Atomen und zumindest 4 bzw. 3 C-Atomen zwischen den zwei freien Valenzen oder Cycloalkylen-alkylen oder p = 0 und L an T gebundenes C 6-11 -Alkenylen oder C 6-11 -Alkadienylen, M Thienylen, Pyridylen, gegebenenfalls substituiertes 1,4-Phenylen oder eine Gruppe der Formeln q 1 oder 0, T CO, CH(R 3 ), C(R 4 ,R 5 ) oder C=NOR 6 und, falls M eine Gruppe M 1 und q = 0 ist, T auch SO 2 sein kann, R 3 OH, F, Alkoxy oder Alkanoyloxy, R 4 OH und R 5 Alkyl, Alkenyl, Alkinyl, Cycloalkyl oder CF 3 oder R 4 zusammen mit R 5 die Gruppe CH 2 , CH 2 O oder CH 2 CH 2 , R 6 H, Alkyl oder Alkenyl, Q Cycloalkyl, C(R 7 ,R 8 ), gegebenenfalls substituiertes Phenyl oder eine geradkettige Alkyl-, Alkenyl-, Alkadienyl- oder Alkatrienylgruppe Q' mit 0 bis 3 Methylsubstituenten und insgesamt 6 bis 13 C-Atomen und R 7 und R 8 C 5-11 -Alkyl, C 5-11 -Alkenyl oder C 5-11 -Alkadienyl sind, und Säureadditionssalze davon haben antimykotische und cholesterinsenkende Wirksamkeit.Tertiary amines of the formula wherein A 1 Alkyl or alkenyl and A 2 Cycloalkyl, cycloalkyl-alkyl or an optionally substituted alkyl or alkenyl group and, if A 1 is alkyl, A 2 can also be OH, A 3 and A 4 Are hydrogen or alkyl or A 1 together with A 2 or with A 3 forms an optionally substituted alkylene, alkenylene or alkadienylene group A 1 -A 2 or A 1 -A 3 , where in a group A 1 -A 2 or A 1 -A 3 up to 2 C atoms can be replaced by one (or two) N atoms and / or by a group N-alkyl, p = 1 and L Phenylene or directly or via O, NH or N (alkyl or alkanoyl) alkylene or alkenylene bonded to M with a total of up to 11 carbon atoms and at least 4 or 3 carbon atoms between the two free valences or cycloalkylene-alkylene or p = 0 and L at T bonded C 6-11 alkenylene or C 6-11 alkadienylene, M Thienylene, pyridylene, optionally substituted 1,4-phenylene or a group of the formula q 1 or 0, T CO, CH (R 3 ), C (R 4 , R 5 ) or C = NOR 6 and, if M is a group M 1 and q = 0, T can also be SO 2 , R 3 OH, F, alkoxy or alkanoyloxy, R 4 OH and R 5 Alkyl, alkenyl, alkynyl, cycloalkyl or CF 3 or R 4 together with R 5 the group CH 2 , CH 2 O or CH 2 CH 2 , R 6 H, alkyl or alkenyl, Q Cycloalkyl, C (R 7 , R 8 ), optionally substituted phenyl or a straight-chain alkyl, alkenyl, alkadienyl or alkatrienyl group Q 'with 0 to 3 methyl substituents and a total of 6 to 13 C atoms and R 7 and R 8 Are C 5-11 alkyl, C 5-11 alkenyl or C 5-11 alkadienyl, and acid addition salts thereof have antifungal and cholesterol-lowering activity.
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Total number of triples: 1409.