Реакция #2878

ord-d45dd22efe384d6e8d41b31969ccab08

Уравнение реакции

Nc1ccc(Br)cc1
4-bromoaniline
O=C(Cl)C=Cc1ccccc1
cinnamoyl chloride
Clc1ccc2cc(Br)ccc2n1
title compound
Clc1ccc2cc(Br)ccc2n1
2-Chloro-6-bromoquinoline
O=c1ccc2cc(Br)ccc2[nH]1
6-bromo-1H-quinolin-2-one

Реагенты

Нет

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Методика

The title compound is prepared from 4-bromoaniline and cinnamoyl chloride according to the procedure described in J. Chem. Soc., Perkin Trans. I, 1972, 1648. The crude 6-bromo-1H-quinolin-2-one intermediate obtained is triturated in Et2O/hexanes and filtered to give a beige solid which is used directly in the chlorination step. The crude product is recrystallized in MeOH to afford the title compound as a beige solid.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05731315uspto-grants-1998_03