HRID2248145
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
1.6 g (0.00331 mole) (+)-1,4-dihydro-5-isopropoxy-2-methyl-4-(2-trifluoromethylphenyl)-1,6-naphthyridine-3-carboxylic acid benzyl ester is taken up in 32 mL ethanol and hydrogenated without the use of pressure at 20° C. in the presence of 0.64 g 10% palladium/charcoal (50% moist). The catalyst is filtered off and the filtrate evaporated to dryness at 35° C. on a rotary evaporator. The solid residue is recrystallized from 10 mL diisopropyl ether. The product is dried at 40° C. in a vacuum drying cabinet; yield: 1.04 g (80.3% of theory).
WORKUP
后处理
- filtrationThe catalyst is filtered off
- customthe filtrate evaporated to dryness at 35° C. on a rotary evaporator
- customThe solid residue is recrystallized from 10 mL diisopropyl ether
- customThe product is dried at 40° C. in a vacuum
- customdrying cabinet