反应 #2122481

ord-12db9e4a17a34c36982881ee8abcb862

反应方程式

Cc1ccc(C)c(CC(=O)Cl)c1
(2,5-dimethyl-phenyl)-acetyl chloride
CCOC(=O)C1(O)CCN(OC)CC1
4-hydroxy-1-methoxy-piperidine-4-carboxylic acid ethyl ester
CN(C)c1ccncc1.CN(C)c1ccncc1
4-dimethylaminopyridine DMAP
CCOC(=O)C1(OC(=O)Cc2cc(C)ccc2C)CCN(OC)CC1
4-[2-(2,5-dimethyl-phenyl)-acetoxy]-1-methoxy-piperidine-4-carboxylic acid ethyl ester

溶剂

反应条件

温度
0°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度The reaction mixture was warmed up to room temperature
  2. 2
    workup.WAITleft
  3. 3
    浓缩Then the reaction mixture was concentrated
  4. 4
    其他the crude product was purified by column chromatography on silica gel (ethyl acetate/cyclohexane first 1:15

实验过程

To a solution of 4-hydroxy-1-methoxy-piperidine-4-carboxylic acid ethyl ester (1.0 g, 4.92 mmol) in 10 ml pyridine under argon was added 4-dimethylaminopyridine DMAP (30 mg, 0.25 mmol). The solution was cooled down to 0° C., then (2,5-dimethyl-phenyl)-acetyl chloride (0.99 g, 5.4 mmol) was added dropwise. The reaction mixture was warmed up to room temperature and left stirring for 5 days. Then the reaction mixture was concentrated and the crude product was purified by column chromatography on silica gel (ethyl acetate/cyclohexane first 1:15, then 1:9) to give pure 4-[2-(2,5-dimethyl-phenyl)-acetoxy]-1-methoxy-piperidine-4-carboxylic acid ethyl ester (compound P3.2) as light yellow oil. Yield: 530 mg.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08574607B2uspto-grants-2013_11