HRID1486707
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 is prepared according to the reactions described for BB-5 above starting from 2-methyl-3-nitro-benzaldehyde and piperidine-4-carboxylic acid tert-butylamide yielding after reductive amination 1-(2-methyl-3-nitro-benzyl)-piperidine-4-carboxylic acid tert-butylamide; LC-MS A: tR=0.62 min; [M+H]+=334.32 followed by reduction with stannous chloride the title compound; LC-MS A: tR=0.45 min; [M+H]+=304.32.
WORKUP
后处理
- customThe title compound is prepared