HRID502418
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
In analogy to the procedure described in example 50k), 2,6-dimethyl-N-piperidin-4-yl-terephthalamic acid [prepared from 4-(4-tert-butoxycarbonyl-3,5-dimethyl-benzoylamino)-piperidine-1-carboxylic acid tert-butyl ester and trifluoroacetic acid in dichloromethane in analogy to the procedure described in example 50i)] was reacted with 3,5-diisopropoxy-benzaldehyde [prepared from 3,5-dihydroxy-benzaldehyde and 2-bromopropane, potassium carbonate in DMF at 60° C. in analogy to the procedure described in example 50e)], sodium cyanoborohydride, N-ethyl-diisopropylamine and acetic acid in ethanol at 50° C. to yield the title compound as light yellow solid. MS: 483.3 (MH+).
WORKUP
后处理
- customat 50° C.