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
CONDITIONS
反应条件
- 温度
- 62.5 °C
PROCEDURE
实验过程
In a 100 mL three neck flask IPA (27 mL) and Dibenzoyl-L-tartaric acid monohydrate (1.84 g) were taken. It was heated to 60-65° C. 4-oxo-4-[3-(trifluoromethyl)-5,6-dihydro[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl]-1-(2,4,5-trifluorophenyl)butan-2-amine (2.0 g, % purity-93.8%) dissolved in methanol (17 mL) was added into reaction mixture at 60-65° C. It was stirred for 60 min. at 60-65° C. Solid salt was precipitated. It was gradually cooled to room temperature over a period of 2-3 h. The salt was filtered and washed with a mixture of IPA: MeOH (2:1). An enantiomerically enriched desired Dibenzoyl-L-tartaric acid salt of mixture of (2R) and (2S)-4-oxo-4-[3-(trifluoromethyl)-5,6-dihydro[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl]-1-(2,4,5-trifluorophenyl)butan-2-amine was obtained (Wt.-0.65 g, % Y-17%, Purity by HPLC-99.8%, % Chiral purity by HPLC of R-isomer 77. %).
WORKUP
后处理
- additionwas added into reaction mixture at 60-65° C
- customSolid salt was precipitated
- temperatureIt was gradually cooled to room temperature over a period of 2-3 h
- filtrationThe salt was filtered
- washwashed with a mixture of IPA: MeOH (2:1)
- additionAn enantiomerically enriched desired Dibenzoyl-L-tartaric acid salt of mixture of (2R)