反応 #5050

ord-cd278516758a47cb98650ef6509a3367

反応方程式

CCOC(=O)c1ccc2[nH]cc(CCCCN)c2c1
3-(4-aminobutyl)-5-ethoxycarbonylindole
CCOC(=O)c1ccc2[nH]ccc2c1
5-ethoxycarbonylindole
O=C(Cl)CCCCl
4-chlorobutyryl chloride
CCOC(=O)c1ccc2[nH]cc(CCCCCl)c2c1
3-(4-chlorobutyl)-5-ethoxycarbonylindole
CCOC(=O)c1ccc2[nH]cc(CCCCN3C(=O)c4ccccc4C3=O)c2c1
3(4-phthalimidobutyl)-5-ethoxycarbonylindole
c1ccc2c(c1)OCCO2
1,4-benzodioxane

反応条件

詳細条件
See reaction.notes.procedure_details.

実験手順

A mixture of 2.18 g of 3-(4-aminobutyl)-5-ethoxycarbonylindole [obtainable from 5-ethoxycarbonylindole by reaction with 4-chlorobutyryl chloride, reduction of the product to give 3-(4-chlorobutyl)-5-ethoxycarbonylindole and conversion into 3(4-phthalimidobutyl)-5-ethoxycarbonylindole] and one equivalent of 6-N,N-bis(2-chloroethyl)amino)-1,4-benzodioxane ("B") in 40 ml of acetone and 40 ml of water is boiled for 24 hours and worked up in the conventional manner. 6-[4-(4-(5-ethoxycarbonylindol-3-yl)butyl)piperazino]-1,4-benzodioxane is obtained.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05242925uspto-grants-1993_09