反応 #1755462

ord-4aaf099713a549dd9a1a6b9f871eaf25

反応方程式

Cc1cc(C)cc(CC(N)c2cccs2)c1
2-(3,5-dimethyl-phenyl)-1-thiophen-2-yl-ethylamine
Cc1cc(C)cc(CC(N)c2cccs2)c1
2-(3,5-Dimethyl-phenyl)-1-thien-2-yl-ethylamine
CC(=O)OCCN=C=S
acetic acid 2-isothiocyanato-ethyl ester
CC(=O)OCCNC(=S)NC(Cc1cc(C)cc(C)c1)c1cccs1
product
収率 25.7%
CC(=O)OCCNC(=S)NC(Cc1cc(C)cc(C)c1)c1cccs1
Acetic Acid 2-{3-[2-(3,5-dimethyl-phenyl)-1-thien-2-yl-ethyl]-thioureido}-ethyl Ester
収率 25.7%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他evaporated
  2. 2
    その他the residue purified by column chromatography

実験手順

A solution of 2-(3,5-dimethyl-phenyl)-1-thiophen-2-yl-ethylamine (1.4 g, from example 1) and acetic acid 2-isothiocyanato-ethyl ester (0.75 g, prepared according to Collect. Czech. Chem. Commun. 1986, 51, 112-117) in toluene (15 ml) was stirred at room temperature for 12 h, evaporated and the residue purified by column chromatography to yield the product (0.5 g) as a yellowish oil.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07989394B2uspto-grants-2011_08