HRID1480134
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
PROCEDURE
实验过程
The mixture of epimers was synthesized in analogy to Example 63b, using 5-Cyclopropyl-4-((R)-2,2,2-trifluoro-1-methyl-ethoxy)-pyridine-2-carboxylic acid (Example 73a) and 1-Cyclopropyl-1-(5-methyl-[1,2,4]oxadiazol-3-yl)-ethylamine (CAN 1155536-64-3) as starting materials and isolated (135 mg, 70%) as light yellow oil. The mixture of epimers was separated by preparative chiral HPLC (Chiralpak AD, isopropanol/heptane) and the title compound was the first epimer collected and isolated as colorless oil; MS (ESI, m/z): 425.5 (M+H+).
WORKUP
后处理
- additionThe mixture of epimers
- customwas synthesized in analogy to Example 63b
- customisolated (135 mg, 70%) as light yellow oil
- additionThe mixture of epimers
- customwas separated by preparative chiral HPLC (Chiralpak AD, isopropanol/heptane)
- customcollected
- customisolated as colorless oil