反应 #2298638

ord-76dba3afa27c4ad3af5afab28c4025db

反应方程式

CCn1c(CCl)nc2ccccc2c1=O
2-chloromethyl-3-ethyl-4-oxo-3,4-dihydroquinazoline
O=Cc1ccc(O)cc1
4-hydroxybenzaldehyde
O=C([O-])[O-].[K+].[K+]
K2CO3
CCn1c(COc2ccc(C=O)cc2)nc2ccccc2c1=O
title compound
收率 88.0%
CCn1c(COc2ccc(C=O)cc2)nc2ccccc2c1=O
4-[[3-Ethyl-4-oxo-3,4-dihydro-2-quinazolinyl]methoxy]benzaldehyde
收率 88.0%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他that described in preparation 13

实验过程

The title compound (4.24 g, 88%) was prepared from 2-chloromethyl-3-ethyl-4-oxo-3,4-dihydroquinazoline (3.5 g, 15.7 mmol) and 4-hydroxybenzaldehyde (2.10 g, 17.21 mmol) in the presence of K2CO3 (2.38 g, 17.26 mmol) as base by a similar procedure to that described in preparation 13.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: USRE039266E1uspto-grants-2006_09