HRID1056111

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：CC(=O)c1c(F)ccc2nc(C)c(NC3(C)CC3)nc12

HCID89781874

未命名化合物

结构：Cc1nc2ccc(F)c(C(=O)CBr)c2nc1NC(C)(C)C

HCID89781926

未命名化合物

PRODUCTS

生成物

结构：Cc1nc2ccc(F)c(C(=O)CBr)c2nc1NC1(C)CC1

HCID89782136

未命名化合物

收率 56%

PROCEDURE

实验过程

2-Bromo-1-(6-fluoro-2-methyl-3-((1-methylcyclopropyl)amino)quinoxalin-5-yl)ethanone (610) (846 mg, 56% yield) as a light yellow solid was prepared according to the procedure described for Intermediate 605, using 1-(6-fluoro-2-methyl-3-((1-methylcyclopropyl)amino)quinoxalin-5-yl)ethanone (610b) (1.18 g, 4.31 mmol) as the starting material. m/z (ESI, +ve ion) 352.1/354.1 (M+H)+.