反応 #481926

ord-f90fa906160e4322933d49ecb7f0a8bd

反応方程式

Nc1ccc2ncnc(Nc3cccc(Br)c3)c2c1
6-amino-4-[(3-bromophenyl)amino]quinazoline
C/C=C/C(=O)Cl
trans-crotonyl chloride
C/C=C/C(=O)Nc1ccc2ncnc(Nc3cccc(Br)c3)c2c1
title compound
収率 52.0%
C/C=C/C(=O)Nc1ccc2ncnc(Nc3cccc(Br)c3)c2c1
N-[4-[(3-Bromophenyl)amino]quinazolin-6-yl]-E-but-2-enamide
収率 52.0%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他A yellow solid formed upon addition
  2. 2
    ろ過The solid was collected by Buchner filtration after 2.5 hours
  3. 3
    その他sonicated with EtOAc

実験手順

To a solution of 6-amino-4-[(3-bromophenyl)amino]quinazoline (316 mg, 1.0 mmol) in THF (6 mL) stirred under N2 at 0° C. was added trans-crotonyl chloride. A yellow solid formed upon addition. The solid was collected by Buchner filtration after 2.5 hours and sonicated with EtOAc to give the title compound (216 mg, 52%), mp 279-281° C.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US06602863B1uspto-grants-2003_08