HRID1468013

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID2736136

5-(Methanesulfonyl)-2,3-dihydro-1H-indole

C9H11NO2S

结构：CC(C)(C)OC(=O)N1CCC(Oc2ccc(Br)cc2)CC1

HCID46739006

tert-Butyl 4-(4-bromophenoxy)piperidine-1-carboxylate

C16H22BrNO3

PRODUCTS

生成物

结构：CC(C)(C)OC(=O)N1CCC(Oc2ccc(N3CCc4cc(S(C)(=O)=O)ccc43)cc2)CC1

HCID67608798

未命名化合物

PROCEDURE

实验过程

The title compound was prepared by following the similar procedure as described in Intermediate-27 using tert-butyl-4-(4-bromophenoxy)piperidine-1-carboxylate and 5-(methylsulfonyl)indoline (0.11 g, 35%); MS: 373 (M−100).