反应 #10586

反应方程式

N-(tert-butoxycarbonyl)-1,3-propylenediamine

triethylamine

isoquinoline-5-sulfonyl chloride

→

title compound

N-(tert-butoxycarbonyl)-N′-[(5-isoquinolyl)sulfonyl]-1,3-propylenediamine

溶剂

dichloromethane

dichloromethane

反应条件

后处理

1. 1
   其他prepared
2. 2
   洗涤The reaction mixture was washed successively with saturated aqueous sodium hydrogencarbonate and saturated brine
3. 3
   其他The organic layer was dried
4. 4
   其他the solvent was evaporated under reduced pressure
5. 5
   其他Then, the residue was purified by flash column chromatography (chloroform:methanol=50:1)

实验过程

A solution of N-(tert-butoxycarbonyl)-1,3-propylenediamine (2.09 g, Tokyo Kasei Kogyo) and triethylamine (3.4 ml, Tokyo Kasei Kogyo) in dichloromethane (20 ml) was added with a solution of isoquinoline-5-sulfonyl chloride (2.73 g, prepared according to Japanese Patent Unexamined Publication (Kokai) No. 61-227581) in dichloromethane (15 ml) with stirring and ice cooling and stirred at room temperature for 14 hours and 30 minutes. The reaction mixture was washed successively with saturated aqueous sodium hydrogencarbonate and saturated brine. The organic layer was dried, and then the solvent was evaporated under reduced pressure. Then, the residue was purified by flash column chromatography (chloroform:methanol=50:1) to obtain the title compound (4 g).

来源