HRID928326

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID15302979

未命名化合物

2 次

结构：Nc1nccn2c([C@@H]3CCCCN3)nc(-c3ccc(C(=O)Nc4ccccn4)cc3)c12

HCID71225973

未命名化合物

2 次

PRODUCTS

生成物

结构：COC/C=C/C(=O)N1CCCC[C@H]1c1nc(-c2ccc(C(=O)Nc3ccccn3)cc2)c2c(N)nccn12

HCID86720313

未命名化合物

收率 54.3%

PROCEDURE

实验过程

This compound was prepared, in an analogous manner as described in Example 2, from (S)-4-(8-amino-3-(piperidin-2-yl)imidazo[1,5-a]pyrazin-1-yl)-N-(pyridin-2-yl)benzamide (intermediate 21) and (E)-4-methoxybut-2-enoic acid (intermediate 3), to afford the title compound (21.1 mg, 54.3%). Data: LCMS (B) Rt: 2.22 min; m/z 512.3 (M+H)+.

WORKUP

后处理

customThis compound was prepared, in an analogous manner