Synthesis of 6-amino-2-(<i>p</i>-aminophenyl)-4-phenylquinazoline

Authors

  • В. Ф. Седова Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk 630090
  • О. П. Шкyрко Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk 630090

Abstract

A study was carried out on the amination of 6-chloro-2-arylquinazolines. The reaction of p-chlorophenyl- and p-nitrophenyl derivatives gives a mixture of mono- and diamination products with predominance of the monoamino products. The desired diamine was also obtained in the reduction of 6-amino-2-(p-nitrophenyl)quinazoline.

How to Cite
Sedova, V. F.; Shkurko, O. P. Chem. Heterocycl. Compd. 1995, 31, 481. [Khim. Geterotsikl. Soedin. 1995, 547.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF01177022

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Published

1995-04-25

Issue

No. 4 (1995)

Section

Original Papers