反应 #170491

ord-db8599ee45fd4b688048ae0a8b0c8ccc

反应方程式

Cc1onc(-c2ccccc2)c1COc1ccc(N)cn1
6-(5-methyl-3-phenyl-isoxazol-4-ylmethoxy)-pyridin-3-ylamine
COC(=O)C(=O)Cl
methyloxalylchloride
COC(=O)C(=O)Nc1ccc(OCc2c(-c3ccccc3)noc2C)nc1
title compound
收率 60.0%
COC(=O)C(=O)Nc1ccc(OCc2c(-c3ccccc3)noc2C)nc1
N-[6-(5-Methyl-3-phenyl-isoxazol-4-ylmethoxy)-pyridin-3-yl]-oxalamic acid methyl ester
收率 60.0%

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

As described for example 179b, 6-(5-methyl-3-phenyl-isoxazol-4-ylmethoxy)-pyridin-3-ylamine (150 mg, 0.53 mmol) was converted, using methyloxalylchloride instead of acetyl chloride, to the title compound (118 mg, 60%) which was obtained as a white solid after purification by chromatography (SiO2, dichloromethane:methanol=100:0 to 9:1). MS: m/e=368.0 [M+H]+.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08846719B2uspto-grants-2014_09