반응 #657288

ord-611e8a3fc24046bfa009511781e43ba6

반응 방정식

Cl
HCl
CNC1(C(=O)OC)CCN(OC)CC1
1-methoxy-4-methylamino-piperidine-4-carboxylic acid methyl ester
Cc1ccc(C)c(CC(=O)Cl)c1
(2,5-dimethyl-phenyl)-acetyl chloride
COC(=O)C1(N(C)C(=O)Cc2cc(C)ccc2C)CCN(OC)CC1
4-{[2-(2,5-dimethyl-phenyl)-acetyl]-methyl-amino}-1-methoxy-piperidine-4-carboxylic acid methyl ester

반응 조건

온도
0°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONpoured on ice water
  2. 2
    기타The layers were separated
  3. 3
    추출the aqueous phase extracted with ethyl acetate (3×25 ml)
  4. 4
    세척the combined organic phases washed with water (3×15 ml) and brine
  5. 5
    건조dried over sodium sulfate
  6. 6
    농축concentrated
  7. 7
    기타The residue was purified by chromatography on silica gel (cyclohexane/ethyl acetate 2:1)

실험 절차

To a solution of 1-methoxy-4-methylamino-piperidine-4-carboxylic acid methyl ester (200 mg, 0.99 mmol) in pyridine (5 ml) was added (2,5-dimethyl-phenyl)-acetyl chloride (240 mg, 1.31 mmol) dropwise at 0° C. The reaction mixture was stirred at 0° C. for one hour and at room temperature for 6 hours, poured on ice water, acidified to pH 7 with an aqueous 2N HCl solution and diluted with ethyl acetate (50 ml). The layers were separated, the aqueous phase extracted with ethyl acetate (3×25 ml), the combined organic phases washed with water (3×15 ml) and brine, dried over sodium sulfate and concentrated. The residue was purified by chromatography on silica gel (cyclohexane/ethyl acetate 2:1). Yield: 170 mg of 4-{[2-(2,5-dimethyl-phenyl)-acetyl]-methyl-amino}-1-methoxy-piperidine-4-carboxylic acid methyl ester (title compound P4.46) as a colorless gum.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09023760B2uspto-grants-2015_05