HRID903586

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID6088

N-Methyltryptamine

C11H14N2

HCID73916

Methyl 4-chloroformylbutyrate

C6H9ClO3

PRODUCTS

生成物

结构：COC(=O)CCCC(=O)N(C)CCc1c[nH]c2ccccc12

HCID23336480

未命名化合物

收率 92.9%

PROCEDURE

实验过程

10.3 g of N-methyl-tryptamine (i.e., 3-(2-methylaminoethyl)-indole) and 11.7 g of 4-methoxycarbonylbutyryl chloride were treated in the same manner as described in Example 1. 16.6 g of N-methyl-N-(4-methoxycarbonylbutyryl)-tryptamine (i.e., 3-[2-(N-methyl-4-methoxycarbonylbutanamido)ethyl]indole) were therby obtained. Yield: 92.8%