Issue 9, 1970

Novel 2-amino-3-pyrazol-5-yl-pyridines from the reaction of 5-chloro-1,8-naphthyridines with hydrazine hydrate and their cyclisation to pyrazolo[1,5-c]pyrido[3,2-e]pyrimidines, a new ring system

Abstract

5-Chloro-1,8-naphthyridines react with hydrazine hydrate to give 2-amino-3-pyrazol-5-yl-pyridines, which can form pyrazolo [1,5-c]pyrido[3,2-e]pyrimidines with triethyl ortho-esters.

Article information

Article type
Paper

J. Chem. Soc. D, 1970, 565a-565a

Novel 2-amino-3-pyrazol-5-yl-pyridines from the reaction of 5-chloro-1,8-naphthyridines with hydrazine hydrate and their cyclisation to pyrazolo[1,5-c]pyrido[3,2-e]pyrimidines, a new ring system

R. A. Bowie, J. Chem. Soc. D, 1970, 565a DOI: 10.1039/C2970000565A

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