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HRID2112443

反应详情

EQUATION

反应方程式

HRID 2112443 的结构方程式

REACTANTS

反应物

2
结构：Cc1cc(C)c(S(=O)(=O)Cl)c(C)c1
HCID13046

2-Mesitylenesulfonyl chloride

C9H11ClO2S

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：Cc1cc(C)c(S(=O)(=O)n2ccc3c(N4CCNCC4)cccc32)c(C)c1.Cl
HCID10295599

未命名化合物

PROCEDURE

实验过程

The title compound was prepared from 4-(4-boc-piperazinyl)-indole and mesitylsulfonylchloride according to Method 3: 1H NMR (270 MHz, DMSO-d6) δ 9.10 (br, 1H), 7.71 (d, J=5 Hz, 1H), 7.40-7.20 (m, 3H), 7.00-6.80 (m, 2H), 6.51 (d, J=8 Hz, 1H), 3.30-3.20 (m, 8H), 2.41 (s, 6. H), 2.27 (s, 3H); MS (ESI+) for m/z 384 (M+H)+.