Author:
Bailey TS,Bremner JB,Pelosi L,Skelton BW,White AH
Abstract
N-Methylation of 6,7-dimethoxy-1-(2�-phenylcyclopropyl)-3,4-dihydroisoquinoline (3b) with iodomethane in refluxing acetone gave the modified Cloke rearrangement product, 8,9-dimethoxy-4-methyl-3-phenyl-2,3,5,6-tetrahyropyrrolo[2,1-a] isoquinolinium iodide (5b), a new derivative of the pyrrolo [2,1-a] isoquinoline skeleton, together with the methiodide salt (4b) of (3b). The structure of (5b) was confirmed by X-ray crystallographic analysis.
Cited by
3 articles.
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