HRID2365400

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：Cn1c2c(c3ccc(Br)cc31)CN(C(=O)OC(C)(C)C)CC2

HCID57950375

tert-Butyl 7-bromo-5-methyl-3,4-dihydro-1H-pyrido[4,3-b]indole-2(5H)-carboxylate

C17H21BrN2O2

HCID58093431

未命名化合物

PRODUCTS

生成物

结构：Cn1c2c(c3ccc(N4CCN(CCc5ccccn5)CC4=O)cc31)CN(C(=O)OC(C)(C)C)CC2

HCID67986819

未命名化合物

收率 56.4%

PROCEDURE

实验过程

tert-Butyl 7-bromo-5-methyl-3,4-dihydro-1H-pyrido[4,3-b]indole-2(5H)-carboxylate (280 mg, 0.761 mmol) and 4-(2-(pyridin-2-yl)ethyl)piperazin-2-one (156 mg, 0.760 mmol) were reacted according to Example 2 (step f) to provide the title compound (210 mg, 56%) as a yellow oil: ESI MS m/z 490 [M+H]+.