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HRID2112448

反应详情

EQUATION

反应方程式

HRID 2112448 的结构方程式

REACTANTS

反应物

2
结构：O=S(=O)(Cl)c1ccc(-c2ccccc2)cc1
HCID74192

(1,1'-Biphenyl)-4-sulphonyl chloride

C12H9ClO2S

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)(c1ccc(-c2ccccc2)cc1)n1ccc2c(N3CCNCC3)cccc21
HCID10226082

未命名化合物

PROCEDURE

实验过程

The title compound was prepared from 4-(4-boc-piperazinyl)-indole and 1,1′-biphenyl-4-ylsulfonyl chloride according to Method 3: 1H NMR (270 MHz, DMSO-d6) δ 9.26 (br, 1H), 8.04 (m, 2H), 7.88 (m, 3H), 7.67 (m, 3H), 7.46 (m, 3H), 7.27 (t, J=8 Hz, 1H), 6.96 (d, J=5 Hz, 1H), 6.80 (d, J=8 Hz, H), 3.25 (m 8H); MS (ESI+) for m/z 418 (M+H)+.