Chemical and Pharmaceutical Bulletin
Online ISSN : 1347-5223
Print ISSN : 0009-2363
ISSN-L : 0009-2363
Photochemical Synthesis of a Pyridopyrrolo [2, 1-α] isoindole System by Cyclization of N-Methylpyridylphthalimides
MASANAO TERASHIMAKOICHI SEKIKOICHI KOYAMAYUICHI KANAOKA
Author information
JOURNAL FREE ACCESS

1977 Volume 25 Issue 7 Pages 1591-1595

Details
Abstract
Photochemical reactions of N-methylpyridylphthalimides (VII-IX) were investigated. Although irradiation of VII in an acetone solution gave only the dihydro product, 3-hydroxy-2-(3-methyl-2-pyridyl) phthalimidine (X), VIII afforded the expected cyclized product, 10b, 11-dihydro-10b-hydroxy-6H-pyrido [4', 3' : 4, 5] pyrrolo [2, 1-a] isoindol-6-one (XII) and dihydro product, 3-hydroxy-2-(4-methyl-3-pyridyl) phthalimidine (XI). Under similar conditions, the cyclized product, 10b, 11-dihydro-10b-hydroxy-6H-pyrido [3', 4' : 4, 5]-pyrrolo [2, 1-a] isoindol-6-one (XIII) was obtained from the photolysis of IX and none of the reduced product was isolated.
Content from these authors
© The Pharmaceutical Society of Japan
Previous article Next article
feedback
Top