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HRID2112450

反应详情

EQUATION

反应方程式

HRID 2112450 的结构方程式

REACTANTS

反应物

2
结构：O=S(=O)(Cl)c1cc(Cl)ccc1Cl
HCID79401

Benzenesulfonyl chloride, 2,5-dichloro-

C6H3Cl3O2S

结构：CC(C)(C)OC(=O)N1CCN(c2cccc3[nH]ccc23)CC1
HCID22015386

tert-Butyl 4-(1H-indol-4-yl)piperazine-1-carboxylate

C17H23N3O2

PRODUCTS

生成物

1
结构：Cl.O=S(=O)(c1cc(Cl)ccc1Cl)n1ccc2c(N3CCNCC3)cccc21
HCID22015371

未命名化合物

PROCEDURE

实验过程

The title compound was prepared according from 4-(4-boc-piperazinyl)-indole and 2,5-dichlorophenylsulfonyl chloride according to Method 3: 1H NMR (270 MHz, DMSO-d6) δ 9.09 (br, 1H), 8.25 (d, J=3 Hz, 1H), 7.91-7.81 (m, 2H), 7.72 (d, J=8 Hz, 1H), 7.36 (d, J=8 Hz, 1H), 7.23 (t, J=8 Hz, 1H), 6.98 (d, J=3 Hz, 1H), 6.82 (d, J=8 Hz, 1H), 3.26 (m, 8H).