Synthesis and alkylation of pyrazolo[3,4-c]isoquinolines and hexahydrocyclohepta[d]pyrazolo[3,4-b]pyridines View Full Text


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Article Info

DATE

2013-09

AUTHORS

I. V. Dyachenko, E. B. Rusanov, M. V. Vovk

ABSTRACT

The condensation of 1-acyl-2-(morpholin-4-yl)cycloalkenes with 3-amino-1-phenyl-1H-pyrazol-5(4H)-ones gave the corresponding 2,3,6,7,8,9-hexahydropyrazolo[3,4-c]isoquinoline and 3,6,7,8,9,10-hexahydrocyclohepta[ d]pyrazolo[3,4-b]pyridine derivatives. Alkylation of 2,3,6,7,8,9-hexahydropyrazolo[3,4-c]-isoquinolines with alkyl halides occurred at the nitrogen atom in the 3-position. The structure of 7-methyl-2,5-diphenyl-2,3,6,7,8,9-hexahydro-1H-pyrazolo[3,4-c]isoquinolin-1-one was proved by X-ray analysis.

PAGES

1364-1368

Identifiers

URI

http://scigraph.springernature.com/pub.10.1134/s1070428013090224

DOI

http://dx.doi.org/10.1134/s1070428013090224

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1023265707


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