反应详情

A suspension of (5-bromo-4-fluoro-2-methyl-phenyl)-acetic acid (8.0 g) and 1,1′-carbonyldiimidazole (5.8 g) in tetrahydrofuran (150 ml) is heated at reflux for 30 minutes. Upon cooling to room temperature, triethylamine (9.0 ml) and 4-amino-1-methoxy-piperidine-4-carboxylic acid methyl ester hydrochloride salt (13.8 g) are added and warming at reflux is continued for 3 hours. The cold reaction mixture is poured on water/ethyl acetate, the layers separated, the organic phase washed with brine, dried over sodium sulfate and concentrated. The residue is solubilised in ethyl acetate/cyclohexane 3:1 and purified by filtration on alumina. Yield: 6.83 g of 4-[2-(5-bromo-4-fluoro-2-methyl-phenyl)-acetylamino]-1-methoxy-piperidine-4-carboxylic acid methyl ester as a solid, mp: 192-193° C.

1. temperatureis heated
2. temperatureat reflux for 30 minutes
3. temperaturewarming
4. temperatureat reflux
5. customThe cold reaction mixture
6. additionis poured on water/ethyl acetate
7. customthe layers separated
8. washthe organic phase washed with brine
9. dry with materialdried over sodium sulfate
10. concentrationconcentrated
11. filtrationpurified by filtration on alumina