Reacción #2298642

ord-74e45c2aacaa4eaca9e0b2f3f32f996e

Ecuación de reacción

CCc1nc(C)cc(=O)[nH]1
2-ethyl-4-methyl-1,6-dihydro-6-pyrimidone
O=[N+]([O-])c1ccc(OCCBr)cc1
4-[2-bromoethoxy]nitrobenzene
[Br-].[Li+]
LiBr
[H-].[Na+]
NaH
CCc1nc(C)cc(=O)n1CCOc1ccc([N+](=O)[O-])cc1
title compound
Rendimiento 30.9%
CCc1nc(C)cc(=O)n1CCOc1ccc([N+](=O)[O-])cc1
4-[2-[2-Ethyl-4-methyl-6-oxo-1,6-dihydro-1-pyrimidinyl]ethoxy]nitrobenzene
Rendimiento 30.9%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrothat described in preparation 1

Procedimiento

The title compound (5.2 g, 25%) was prepared from 2-ethyl-4-methyl-1,6-dihydro-6-pyrimidone (7.65 g, 55.43 mmol), 4-[2-bromoethoxy]nitrobenzene (15.0 g, 60.97 mmol), LiBr (11.09 g, 127.49 mmol) and 60% NaH (2.76 g, 72.06 mmol) as base by a similar procedure to that described in preparation 1.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: USRE039266E1uspto-grants-2006_09