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Methanol → 2-(4-Bromo-phenyl)-3-(1-methyl-piperidin-4-yl)-propionic acid methyl ester

HRID 220181
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HRID 220181 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([CH2:12][CH:13]2[CH2:18][CH2:17][N:16]([CH3:19])[CH2:15][CH2:14]2)[C:9]([OH:11])=[O:10])=[CH:4][CH:3]=1.[CH3:20]O>O=S(Cl)Cl>[CH3:20][O:10][C:9](=[O:11])[CH:8]([C:5]1[CH:4]=[CH:3][C:2]([Br:1])=[CH:7][CH:6]=1)[CH2:12][CH:13]1[CH2:14][CH2:15][N:16]([CH3:19])[CH2:17][CH2:18]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 887MethanolHCID 592383282-(4-Bromo-phenyl)-3-(1-methyl-piperidin-4-yl)-propionic acid

생성물 1

HCID 592382632-(4-Bromo-phenyl)-3-(1-methyl-piperidin-4-yl)-propionic acid methyl ester

시약·촉매·용매 1

HCID 24386Thionyl Chloride용매

실험 절차

To the solution of 2-(4-bromo-phenyl)-3-(1-methyl-piperidin-4-yl)-propionic acid in MeOH (60 mL), SOCl2 (2 mL) was added at 0 degrees Celsius, then the mixture refluxed for 5 h. After cooling, the solution was evaporated to dryness under reduced pressure, then EtOAc was added, the organic layer was washed with aq. NaHCO3, dried with MgSO4, and evaporated to give an oil. MS: calc'd 340 (MH+), exp 340 (MH+).

후처리

  1. temperaturethe mixture refluxed for 5 h
  2. temperatureAfter cooling
  3. customthe solution was evaporated to dryness under reduced pressure
  4. additionEtOAc was added
  5. washthe organic layer was washed with aq. NaHCO3
  6. dry with materialdried with MgSO4
  7. customevaporated
  8. customto give an oil

출처 및 근거

ORD 기록
ord-b31573fe8baf4f359d74fd72be05e16c
출처 데이터셋
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08202866B2

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