| 摘要 |
Isoquinolines a (R2, R3 independently = H, alkyl, cycloalkyl, alkenyl, acyl, aryl, aralkyl; R4=alkyl, hydroxy-, phhydroxy-, halophenylhydroxy-, alkylphenylhydroxy-, aryloxyhydroxy- alkoxyhydroxy-, acyloxy-, arylcarbonyl-, alkoxycarbonyl-, alkylcyclo-, thienyl-, furyl-, aryl carbox amido-, cyclic alkylox-, cyclic alkylhydroxy-, alkenyloxy-, aryloxy-, N-alkylpyrrolidinyl-, aryl-N-imidazolonyl-alkyl, alkynyl, alkenyl; X=O, S) were prepd. Thus, a mixt. contg. 3-ethyl-2-methyl-4, 4a,5,6,8,8a,9-octahydro-lH-pyrrolo[2,3-g -isoquinolin4-thione, K2CO3, and 2-bromoethylbenzene was refluxed for 3 hrs. to give 3-etyl-2 methyl-6-(2-phenylethyl)-4,4a,5,6,7,8,8a, 9-octahydro-4a, 8a trans-lH-pyrrolo[2,3-g isoquinolin-4-thione.
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