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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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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 482925
[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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Komponenten

8

Edukt 5

HCID 6371PhosgeneHCID 8471Triethylamine2×HCID 218852-DimethylaminopyridineHCID 12834624benzyl N-[(3S)-2-oxoazetidin-3-yl]carbamateHCID 15640239N-methyl-DL-alanine, benzyl ester

Produkt 1

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

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 1140TolueneLösungsmittelHCID 6344DichloromethaneLösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

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).

Aufarbeitung

  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

Quellen und Nachweise

ORD-Eintrag
ord-cba0cb31a43d4dd6a17e49c9769038e5
Quelldatensatz
uspto-grants-1986_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04576749

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