反応 #71921

反応方程式

cis(±)-benzyl (1-carbamoyl-3-methoxypiperidin-4-yl)carbamate

butyl 3-bromo-4-methyl-2-oxobutanoate

Butyl 3-bromo-4-methyl-2-oxobutanoate

sodium bicarbonate

→

title compound

収率 100.0%

Ethyl cis(±)-2-(4-{[(benzyloxy)carbonyl]amino}-3-methoxypiperidin-1-yl)-5-isopropyl-1,3-oxazole-4-carboxylate

収率 100.0%

溶媒

THF

反応条件

後処理

1. 1
   その他The resulting residue was purified by silica gel column chromatography (elution solvent: ethyl acetate/hexane=1/4, 2/3, 1/1, 3/2, 2/1)

実験手順

The same operation as in Example (103c) was performed using cis(±)-benzyl (1-carbamoyl-3-methoxypiperidin-4-yl)carbamate obtained in Example (103b) (0.97 g, 3.16 mmol), butyl 3-bromo-4-methyl-2-oxobutanoate obtained in Example (111a) (7.6 g, 30.2 mmol), sodium bicarbonate (0.7 g, 8.3 mmol) and THF (20 mL). The resulting residue was purified by silica gel column chromatography (elution solvent: ethyl acetate/hexane=1/4, 2/3, 1/1, 3/2, 2/1) to obtain 0.43 g of the title compound as a colorless solid (100%).

出典