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HRID2112453

反应详情

EQUATION

反应方程式

HRID 2112453 的结构方程式

REACTANTS

反应物

2
结构：CS(=O)(=O)c1ccccc1S(=O)(=O)Cl
HCID2735178

2-(methylsulfonyl)benzenesulfonyl chloride

C7H7ClO4S2

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：CS(=O)(=O)c1ccccc1S(=O)(=O)n1ccc2c(N3CCNCC3)cccc21.Cl
HCID10139159

未命名化合物

PROCEDURE

实验过程

The title compound was prepared from 4-(4-boc-piperazinyl)-indole and 2-methylsulfonyl-phenylsulfonyl chloride according to Method 3: 1H NMR (270 MHz, DMSO-d6) δ 9.22 (br, 1H), 8.29 (d, J=8 Hz, 1H), 7.99 (t, J=8 Hz, 1H), 7.90-7.80 (m, 2H), 7.43 (d, J=8 Hz, 1H), 7.30-7.15 (m, 2H), 7.04 (d, J=3 Hz, 1H), 6.85 (d, J=8 Hz, 1H), 3.56 (s, 3H), 3.29 (m, 8H); MS (ESI+) for m/z 420 (M+H)+.