Synthesis of 3,3-disubstituted 2-iminoindolines by cyclization of 1-phenyl-2-acylhydrazines |
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Authors: | A N Kost G A Golubeva V G Zabrodnyaya Yu N Portnov |
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Institution: | (1) M. V. Lomonosov Moscow State University, USSR |
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Abstract: | 3,3-Disubstituted 2-iminoindolines and the corresponding 10,10-disubstituted tetrahydropyrimido-1,2-a] indoles, including compounds with spiran structures, were synthesized by reaction of 1-phenyl-2-acylhydrazines and l-phenyl-2-acylpyrazolidines geminally substituted at the -carbon atom of the acyl residue with phosphorus oxychloride. An instance of cleavage of the methyl group was detected.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 12, pp. 1632–1635, December, 1975. |
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