反应详情

1.9 g of 10-hydroxy-2,3,11-trimethoxy-5,6,13,13a-tetrahydro-8H-dibenzo[a, g]quinolizine hydrochloride was treated in the same manner as described in Example 6, using 2.0 g of 3,4-dimethoxycinnamoyl chloride and 20 ml of anhydrous pyridine and there was obtained 1.0 g (38.4% yield) of 5,6,13,13a-tetrahydro-2,3,11-trimethoxy-10-(3', 4'-dimethoxycinnamoyloxy)-8H-dibenzo[a, g] quinolizine as a pale brown powder. The methiodide derived from this compound was found to be in agreement with the methiodide of the compound obtained in Example 4 as determined from the melting point and IR spectrum.