反应详情

Prepared using the product from Example 13 step b) (0.15 g) and (1R,2S)-2-(3,4-difluorophenyl)cyclopropanamine, (2R,3R)-2,3-dihydroxybutanedioate (1:1) (0.20 g) (prepared as described in WO 9905143) by the method of Example 13, step c). Purified by chromatography (SiO2, ethyl acetate:dichloromethane 1:9 as eluant) to afford the title (0.12 g).

1. customPrepared
2. customPurified by chromatography (SiO2, ethyl acetate:dichloromethane 1:9 as eluant)
3. customto afford the title (0.12 g)