HRID1621609
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
PROCEDURE
实验过程
The title compound was prepared in an analogous manner to that described in Example 155, Step 2, using 5-fluoro-6-methoxypyridin-3-amine and tert-butyl 4-((5-(4-(bis(4-methoxybenzyl)amino)-6-methyl-1,3,5-triazin-2-yl)-6-fluoropyridin-3-yl)methyl)piperazine-1-carboxylate. tert-Butyl 4-((5-(4-(bis(4-methoxybenzyl)amino)-6-methyl-1,3,5-triazin-2-yl)-6-(5-fluoro-6-methoxypyridin-3-ylamino)pyridin-3-yl)methyl)piperazine-1-carboxylate was isolated (90%) as a yellow solid. m/z (ESI, +ve ion) 765.8 (M+H)+.
WORKUP
后处理
- customThe title compound was prepared in an analogous manner to that