反应 #336831

ord-8265653390ae41fc9519cf3970ba4a73

反应方程式

CCOC(OCC)c1cc(=O)nc(C2CC2)[nH]1
2-cyclopropyl-6-(diethoxymethyl)-4(1H)-pyrimidinone
O=C1CCC(=O)N1Br
N-bromosuccinimide
CCOC(=O)c1nc(C2CC2)[nH]c(=O)c1Br
title product
CCOC(=O)c1nc(C2CC2)[nH]c(=O)c1Br
ethyl 5-bromo-2-cyclopropyl-1,6-dihydro-6-oxo-4-pyrimidinecarboxylate

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

To a solution of 2-cyclopropyl-6-(diethoxymethyl)-4(1H)-pyrimidinone (i.e. the title product of Step A) (2.9 g, 12.1 mmol) in dichloromethane (75 mL) was added N-bromosuccinimide (4.76 g, 26.8 mmol). The reaction mixture was stirred overnight. The solvent was removed with a rotary evaporator. The residue was purified by MPLC (1→4% methanol in dichloromethane as eluant) to afford the title compound as a white solid (2.68 g).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07863220B2uspto-grants-2011_01