反应 #83033

反应方程式

ethyl acetoimidate hydrochloride

ethyl acetoimidate hydrochloride

5-(2-amino-ethoxy)-7-chloro-1-[2-methoxy-4-(2-chlorobenzoylamino)-benzoyl]-2,3,4,5-tetrahydro-1H-benzoazepine

→

5-[2-(1-iminoethyl)aminoethoxy]-7-chloro-1-[2-methoxy-4-(2-chlorobenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzo-azepine hydrochloride

收率 69.8%

溶剂

ethanol

反应条件

后处理

1. 1
   温度cooling
2. 2
   workup.STIRRINGThe mixture was stirred at 50° C. for 7 hours
3. 3
   温度refluxed for 3 hours
4. 4
   温度After cooling
5. 5
   过滤the reaction mixture was subjected to filtration
6. 6
   其他to remove insolubles
7. 7
   浓缩The filtrate was concentrated
8. 8
   其他The residue was purified by silica gel column chromatography (elutant: dichloromethane/methanol=30/1)

实验过程

0.129 g of ethyl acetoimidate hydrochloride was added to 15 ml of a suspension of 0.5 g of 5-(2-amino-ethoxy)-7-chloro-1-[2-methoxy-4-(2-chlorobenzoylamino)-benzoyl]-2,3,4,5-tetrahydro-1H-benzoazepine in ethanol with ice-cooling. The mixture was stirred overnight at room temperature. Then, 0.163 g of ethyl acetoimidate hydrochloride was further added. The mixture was stirred at 50° C. for 7 hours and then refluxed for 3 hours. After cooling, the reaction mixture was subjected to filtration to remove insolubles. The filtrate was concentrated. The residue was purified by silica gel column chromatography (elutant: dichloromethane/methanol=30/1) to obtain 0.2 g of 5-[2-(1-iminoethyl)aminoethoxy]-7-chloro-1-[2-methoxy-4-(2-chlorobenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzo-azepine hydrochloride.

来源