反应 #657284

ord-0bcef22479a64fc28b08471dcc3585bf

反应方程式

CNC1(C(=O)O)CCN(OC)CC1.Cl
1-methoxy-4-methylamino-piperidine-4-carboxylic acid hydrochloride salt
CO
methanol
O=S(Cl)Cl
thionyl chloride
CNC1(C(=O)OC)CCN(OC)CC1
1-methoxy-4-methylamino-piperidine-4-carboxylic acid methyl ester

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度the reaction mixture was heated
  2. 2
    温度at reflux for 7 days
  3. 3
    温度After cooling
  4. 4
    浓缩the mixture was concentrated
  5. 5
    workup.ADDITIONthe residue diluted with ice water and neutralised with aqueous sodium bicarbonate
  6. 6
    萃取The aqueous phase was extracted with ethyl acetate (4×)
  7. 7
    洗涤the combined organic layers washed with brine
  8. 8
    干燥dried over sodium sulfate
  9. 9
    浓缩concentrated
  10. 10
    其他The residue was purified by chromatography on silica gel (gradient ethyl acetate→ethyl acetate/methanol 20:1)

实验过程

To a suspension of 1-methoxy-4-methylamino-piperidine-4-carboxylic acid hydrochloride salt (2.08 g, 9.26 mmol) in methanol (20 ml) at 0-5° C. was added thionyl chloride (2.41 ml, 3.97 g, 33.40 mmol) and the reaction mixture was heated at reflux for 7 days. After cooling, the mixture was concentrated, the residue diluted with ice water and neutralised with aqueous sodium bicarbonate. The aqueous phase was extracted with ethyl acetate (4×), the combined organic layers washed with brine, dried over sodium sulfate and concentrated. The residue was purified by chromatography on silica gel (gradient ethyl acetate→ethyl acetate/methanol 20:1). Yield: 76 mg of 1-methoxy-4-methylamino-piperidine-4-carboxylic acid methyl ester (title compound P5.4) as an oil.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US09023760B2uspto-grants-2015_05