Methanol → 4-Hydroxyamino-1-methoxy-piperidine-4-carboxylic acid methyl ester

HRID 1473791노트

반응식

HRID 1473791 반응식
[OH:1][NH:2][C:3]1([C:11]([OH:13])=[O:12])[CH2:8][CH2:7][N:6]([O:9][CH3:10])[CH2:5][CH2:4]1.S(Cl)(Cl)=O.[CH3:18]O>>[CH3:18][O:12][C:11]([C:3]1([NH:2][OH:1])[CH2:8][CH2:7][N:6]([O:9][CH3:10])[CH2:5][CH2:4]1)=[O:13]

참가 물질

4

실험 절차

To a suspension of 4-hydroxyamino-1-methoxy-piperidine-4-carboxylic acid (1.0 g, 5.26 mmol) in methanol (25 ml) at 0-10° C. was added thionyl chloride (1.14 ml, 1.88 g, 15.77 mmol) and the reaction mixture was heated at reflux for 48 hours. After cooling, the mixture was concentrated, the residue diluted with ice water (20 ml) and neutralised with aqueous sodium bicarbonate. The aqueous phase was extracted with diethyl ether (3×25 ml), the combined organic layers washed with aqueous sodium bicarbonate and brine, dried over sodium sulfate and concentrated. Yield: 0.53 g of 4-hydroxyamino-1-methoxy-piperidine-4-carboxylic acid methyl ester (title compound P4ii.2) as a viscous, yellowish oil. This material was identical to the compound described above under preparation ‘EXAMPLE 11, Step 3’.

후처리

  1. temperaturethe reaction mixture was heated
  2. temperatureat reflux for 48 hours
  3. temperatureAfter cooling
  4. concentrationthe mixture was concentrated
  5. additionthe residue diluted with ice water (20 ml)
  6. extractionThe aqueous phase was extracted with diethyl ether (3×25 ml)
  7. washthe combined organic layers washed with aqueous sodium bicarbonate and brine
  8. dry with materialdried over sodium sulfate
  9. concentrationconcentrated
  10. customdescribed above under preparation ‘EXAMPLE 11, Step 3’

출처 및 근거

ORD 기록
ord-c412afc450e244a89538b18655c3584a
출처 데이터셋
uspto-grants-2015_04
특허 번호
US09018135B2

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