A CONVENIENT METHOD FOR THE PREPARATION OF LINEAR FUROQUINOLIN-2-ONES

Authors

  • А. В. Васильев D. I. Mendeleev Russian Chemical-Technological University, Moscow 125047
  • Н. П. Соловьева State Unitary Enterprise, Center for the Chemistry of Medicinal Substances, All-Russia Research Chemical-Pharmaceutical Institute, Moscow 119815
  • Н. Я. Подхалюзина D. I. Mendeleev Russian Chemical-Technological University, Moscow 125047
  • А. Ю. Толмачев D. I. Mendeleev Russian Chemical-Technological University, Moscow 125047
  • В. Ф. Травень D. I. Mendeleev Russian Chemical-Technological University, Moscow 125047

Keywords:

6-acetyl-7-hydroxy-4-methylquinolin-2-one, 3,5-dimethylfuro[3,2-g]quinolin-7-one, Fries rearrangement

Abstract

Fries rearrangement of 7-acetoxy-4-methylquinolin-2-one and subsequent condensation of the 6-acetyl-7-hydroxy-4-methylquinolin-2-one obtained with α-chloro ketones gives a series of furo[3,2-g]quinolin-7-ones.

How to Cite
Vasilyev, A. V.; Solov'eva, N. P.; Podhaluzina, N. Ya.; Tolmachev, A. Yu.; Traven, V. F. Chem. Heterocycl. Compd. 2003, 39, 534. [Khim. Geterotsikl. Soedin. 2003, 618.]

For this article in the English edition, see DOI https://doi.org/10.1023/A:1024729817055

Published

2003-04-25

Issue

Section

Original Papers