反応 #1350570

ord-318c4e9e02ea4fdf9942c5ed5ded83c8

反応方程式

COc1ccc(OC(=O)Cl)cc1
4-methoxyphenylchloroformate
Cn1cc(Br)c(-c2cccc(N)c2)n1
3-(3-aminophenyl)-4-bromo-1-methylpyrazole
CCN(CC)CC
triethylamine
COc1ccc(OC(=O)Nc2cccc(-c3nn(C)cc3Br)c2)cc1
title compound
収率 59.7%
COc1ccc(OC(=O)Nc2cccc(-c3nn(C)cc3Br)c2)cc1
N-[3-(4-bromo-1-methylpyrazol-3-yl)phenyl][4-methoxyphenoxy]carboxamide
収率 59.7%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    濃縮concentrated

実験手順

To 4-methoxyphenylchloroformate (19 mg, 0.10 mmol) in CH2Cl2 (0.5 mL) was added dropwise a solution of 3-(3-aminophenyl)-4-bromo-1-methylpyrazole (25 mg, 0.10 mmol) and triethylamine (14 μL, 0.10 mmol) in CH2Cl2 (0.5 mL). The mixture was stirred for 16 h and concentrated. Chromatography on flash silica (40% EtOAc/hexane) gave the title compound as a colourless solid (24 mg, 526), m.p. 140.3-141.8° C. (EtOAc/hexane).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US06541209B1uspto-grants-2003_04