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Phosgene → (S)-N-[[3-[[(Phenylmethoxy)carbonyl]amino]-2-oxo-1-azetidinyl]carbonyl]N-methyl-DL-alanine, phenylmethyl ester

HRID 482925
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HRID 482925 반응식
[C:1](Cl)(Cl)=[O:2].[CH3:5][NH:6][CH:7]([C:9]([O:11][CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)=[O:10])[CH3:8].C(N(CC)CC)C.[C:26]1([CH2:32][O:33][C:34]([NH:36][C@H:37]2[CH2:40][NH:39][C:38]2=[O:41])=[O:35])[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1.CN(C1C=CC=CN=1)C>C1(C)C=CC=CC=1.ClCCl>[C:26]1([CH2:32][O:33][C:34]([NH:36][CH:37]2[CH2:40][N:39]([C:38]([N:6]([CH3:5])[C@H:7]([C:9]([O:11][CH2:12][C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)=[O:10])[CH3:8])=[O:41])[C:1]2=[O:2])=[O:35])[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1
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8

반응물 5

HCID 6371PhosgeneHCID 8471Triethylamine2회HCID 218852-DimethylaminopyridineHCID 12834624benzyl N-[(3S)-2-oxoazetidin-3-yl]carbamateHCID 15640239N-methyl-DL-alanine, benzyl ester

생성물 1

HCID 131714547(S)-N-[[3-[[(Phenylmethoxy)carbonyl]amino]-2-oxo-1-azetidinyl]carbonyl]N-methyl-DL-alanine, phenylmethyl ester

시약·촉매·용매 2

HCID 1140Toluene용매HCID 6344Dichloromethane용매

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온도
0 °C

실험 절차

A solution of phosgene in toluene (4.7 ml of a 20% solution, 9.36 mmol) was cooled to -25° C. under argon. While stirring, a solution (pre-cooled to 0° C.) of N-methyl-DL-alanine, benzyl ester (1.0 g, 5.2 mmol) and triethylamine (870 μl, 6.25 mmol) in dichloromethane (5 ml) was added over 5 minutes maintaining the temperature at -20° to -25° C. After stirring at -25° C. for 1 hour, solvent and excess phosgene were removed in vacuo. The residue was dissolved in dichloromethane (12 ml), cooled to 0° C. and then (S)-3-[[(phenylmethoxy)carbonyl]amino]-2-azetidinone (1.15 g, 5.2 mmol), dimethylaminopyridine (63 mg, 0.52 mmol), and triethylamine (870 μl, 6.2 mmol) were added sequentially. Stirring was continued for 10 minutes at 0° C. and then overnight at room temperature. After refluxing for an additional 7 hours, the mixture was again stirred overnight at room temperature. The mixture was washed with water, dried (Na2SO4) and solvent was removed in vacuo. The resulting oil was chromatographed on silica gel eluting with a 4:6 ethyl acetate:hexane mixture. The desired product was obtained as an oil (580 mg).

후처리

  1. temperaturemaintaining the temperature at -20° to -25° C
  2. stirringAfter stirring at -25° C. for 1 hour
  3. customsolvent and excess phosgene were removed in vacuo
  4. dissolutionThe residue was dissolved in dichloromethane (12 ml)
  5. stirringStirring
  6. customovernight
  7. customat room temperature
  8. temperatureAfter refluxing for an additional 7 hours
  9. waitthe mixture was again stirred overnight at room temperature
  10. washThe mixture was washed with water
  11. dry with materialdried (Na2SO4) and solvent
  12. customwas removed in vacuo
  13. customThe resulting oil was chromatographed on silica gel eluting with a 4:6 ethyl acetate

출처 및 근거

ORD 기록
ord-cba0cb31a43d4dd6a17e49c9769038e5
출처 데이터셋
uspto-grants-1986_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04576749

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