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Trifluoroacetic acid → 4-[2-Methoxyethylthio]-3,3-diethyl-2-azetidinone

HRID 842424
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HRID 842424 반응식
C1([C:7]([C:19]2[CH:24]=[CH:23]C=[CH:21][CH:20]=2)(C2C=CC=CC=2)[S:8][CH2:9][CH2:10][O:11][CH3:12])C=CC=CC=1.C([SiH](CC)CC)C.FC(F)(F)C(O)=O.[OH-].[Na+].C([O:44][CH:45]1[NH:48]C(=O)C1(CC)CC)(=O)C>ClCCl.CC(C)=O>[CH3:12][O:11][CH2:10][CH2:9][S:8][CH:7]1[NH:48][C:45](=[O:44])[C:19]1([CH2:20][CH3:21])[CH2:24][CH3:23]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 5

HCID 6422Trifluoroacetic acidHCID 12052TriethylsilaneHCID 14798Sodium Hydroxide2회HCID 102618172-Azetidinone, 4-(acetyloxy)-3,3-diethyl-HCID 22614061S-Triphenylmethyl 2-Methoxyethanethiol

생성물 1

HCID 187242294-[2-Methoxyethylthio]-3,3-diethyl-2-azetidinone수율 63%

시약·촉매·용매 2

HCID 180Acetone용매2회HCID 6344Dichloromethane용매

실험 절차

To S-triphenylmethyl 2-methoxyethanethiol (1.37 g, 4.1 mmol) in dichloromethane (30 ml) under nitrogen were added triethylsilane (0.953 g, 1.31 ml, 8.2 mmol) and trifluoroacetic acid (0.632 ml, 0.935 g, 8.2 mmol). The mixture was stirred at room temperature for 16 hours. Acetone (50 ml) was added and the mixture neutralised with 2 M aqueous sodium hydroxide. 1 M Aqueous sodium hydroxide (24 ml, 24 mmol), 4-acetoxy-3,3-diethyl-2-azetidinone (J. Med. Chem., 35, 3745-3754 (1992)) (0.690 g, 6.00 mmol) and acetone (10 ml) were then added and the mixture stirred at room temperature for 23 hours. The solvents were removed in vacuo and to the residue were added water (50 ml) and dichloromethane (50 ml). The organic layer was isolated and the water layer extracted further with dichloromethane (3×30 ml). The 4 organic layers were combined and washed with water (30 ml) and saturated brine (30 ml), dried (Na2SO4) and concentrated in vacuo. Purification by flash column chromatography (gradient from petrol/EtOAc, 9:1 to EtOAc) gave the title compound (0.51 g, 63%) as an oil.

후처리

  1. stirringthe mixture stirred at room temperature for 23 hours
  2. customThe solvents were removed in vacuo and to the residue
  3. additionwere added water (50 ml) and dichloromethane (50 ml)
  4. customThe organic layer was isolated
  5. extractionthe water layer extracted further with dichloromethane (3×30 ml)
  6. washwashed with water (30 ml) and saturated brine (30 ml)
  7. dry with materialdried (Na2SO4)
  8. concentrationconcentrated in vacuo
  9. customPurification by flash column chromatography (gradient from petrol/EtOAc, 9:1 to EtOAc)

출처 및 근거

ORD 기록
ord-e213af0f64364fb2906065bad0713464
출처 데이터셋
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06375926B1

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