反応 #2298633

ord-322faf012671419fa7caa665c10a7f9c

反応方程式

CCc1nc(-c2ccccc2)cc(=O)[nH]1
2-ethyl-4-phenyl-1,6-dihydro-6-pyrimidone
O=Cc1ccc(OCCBr)cc1
4-[2-bromoethoxy]benzaldehyde
[Br-].[Li+]
LiBr
[H-].[Na+]
NaH
CCc1nc(-c2ccccc2)cc(=O)n1CCOc1ccc(C=O)cc1
title compound
収率 44.2%
CCc1nc(-c2ccccc2)cc(=O)n1CCOc1ccc(C=O)cc1
4-[2-[2-Ethyl-4-phenyl-6-oxo-1,6-dihydro-1-pyrimidinyl]ethoxy]benzaldehyde
収率 44.2%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他that described in preparation 1

実験手順

The title compound (2.0 g, 44%) was prepared from 2-ethyl-4-phenyl-1,6-dihydro-6-pyrimidone (2.6 g, 13.0 mmol), 4-[2-bromoethoxy]benzaldehyde (2.97 g, 13.0 mmol) and LiBr (2.59 g, 29.9 mmol) in the presence of NaH as base (0.4 g, 16.9 mmol) by a similar procedure to that described in preparation 1.

出典

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