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HRID1836129

反应详情

EQUATION

反应方程式

HRID 1836129 的结构方程式

REACTANTS

反应物

2
结构：CC1CN(C(=O)CCc2c(C=O)[nH]c3c2CCCC3)CC(C)N1
HCID23498817

未命名化合物

结构：CCS(=O)(=O)c1ccc2c(c1)CC(=O)N2
HCID23498854

未命名化合物

PRODUCTS

生成物

1
结构：CCS(=O)(=O)c1ccc2c(c1)/C(=C/c1[nH]c3c(c1CCC(=O)N1CC(C)NC(C)C1)CCCC3)C(=O)N2
HCID60104770

未命名化合物

收率 46%

PROCEDURE

实验过程

3-[3-(3,5-Dimethylpiperazin-1-yl)-3-oxo-propyl]-4,5,6,7-tetrahydro-1H-indole-2-carbaldehyde, prepared as described in Example 3 above, was condensed with 5-ethylsulfonyloxindole following the same procedure used in example 1 to give the desired product (72 mg, 46% yield).