Реакция #2298646

ord-03b146252fb6447f82bca9653e3bee4a

Уравнение реакции

Cc1nc2ccccc2c(=O)[nH]1
2-methyl-4-oxo-3,4-dihydroquinazoline
O=[N+]([O-])c1ccc(OCCBr)cc1
4-[2-bromoethoxy]nitrobenzene
O=C([O-])[O-].[K+].[K+]
K2CO3
Cc1nc2ccccc2c(=O)n1CCOc1ccc([N+](=O)[O-])cc1
title compound
Выход 60.0%
Cc1nc2ccccc2c(=O)n1CCOc1ccc([N+](=O)[O-])cc1
4-[2-[2-Methyl-4-oxo-3,4-dihydro-3-quinazolinyl]ethoxy]nitrobenzene
Выход 60.0%

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеthat described in preparation 1

Методика

The title compound (1.2 g, 60%) was prepared from 2-methyl-4-oxo-3,4-dihydroquinazoline (1.0 g, 6.25 mmol) and 4-[2-bromoethoxy]nitrobenzene (1.69 g, 6.9 mmol) and K2CO3 (1.73 g, 12.3 mmol) as a base by a similar procedure to that described in preparation 1.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: USRE039266E1uspto-grants-2006_09