SYNTHESIS, ANTICONVULSANT AND ANTIHYPERTENSIVE ACTIVITY OF DIASTEREOMERIC 9,10-DIMETHOXY-1,3,4,6,7,11B-HEXAHYDROSPIRO-[BENZO[A]QUINOLIZIN-2,4'-IMIDAZOLIDINE]-2',5'-DIONES

被引:25
作者
MENENDEZ, JC
DIAZ, MP
BELLVER, C
SOLLHUBER, MM
机构
[1] UNIV COMPLUTENSE MADRID,FAC FARM,DEPT QUIM ORGAN & FARMACEUT,E-28040 MADRID,SPAIN
[2] LAB MORRITH MIGUEL YUSTE,SECC FARMACOL,E-28037 MADRID,SPAIN
[3] UNIV COMPLUTENSE MADRID,FAC FARM,DEPT FARMACOL,E-28040 MADRID,SPAIN
关键词
BENZO[A]QUINOLIZINES; HYDANTOINS; ANTICONVULSANT ACTIVITY; ANTIHYPERTENSIVE ACTIVITY;
D O I
10.1016/0223-5234(92)90062-6
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The synthesis of the 2S, 11bS (2) and 2R, 11bS (3) diastereoisomers of the 9,10-dimethoxy-1,3,4,5,6,11b-hexahydrospiro[benzo[a]quinolizin-2,4'-imidazolidine]-2',5'-dione system was achieved using the Bucherer-Bergs and Read hydantoin syntheses respectively. Alternatively, the 2R, 11bS isomer was prepared by treating the appropriate aminonitrile with chlorosulphonyl isocyanate, followed by acid hydrolysis. Compound 3 showed good anticonvulsant activity against pentamethylenetetrazole-induced seizures. Its behaviour is discussed in comparison with that of phenytoin. Both compounds were inactive as antihypertensives.
引用
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页码:61 / 66
页数:6
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