Реакция #8708

ord-c9c2f8cbb6934fe4be43d947331b2f89

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Экстракцияextracted twice with diethyl ether
  2. 2
    ДругоеThe precipitate was collected
  3. 3
    Промывкаwashed with water and diethyl ether
  4. 4
    Другоеdried

Методика

A solution of 4,6-dichloro-5-(4-chlorophenyl)pyrimidine (848 mg), 2-thiophen-2-yl-ethanesulfonic acid amide potassium salt (1.5 g, Referential Example 14) and Hunig's base (1 ml) in DMSO (20 ml) was stirred at rt for 24 h before it was diluted with water (200 ml) and extracted twice with diethyl ether. The aqueous layer was acidified with acetic acid. The precipitate was collected, washed with water and diethyl ether and dried to give 2-thiophen-2-yl-ethanesulfonic acid [6-chloro-5-(4-chloro-phenyl)-pyrimidin-4-yl]-amide (930 mg) as a beige powder. LC-MS: tR=5.01 min, [M+1]+=413.49, [M−1]−=411.93.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07091201B2uspto-grants-2006_08