StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

Phosgene → (3S-trans)-N-[[3-[[t-Butoxycarbonyl]amino]-4-methyl-2-oxo-1-azetidinyl]carbonyl]-N-methylglycine, t-butyl ester

HRID 482926
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 482926
[C:1](Cl)(Cl)=[O:2].[CH3:5][NH:6][CH2:7][C:8]([O:10][C:11]([CH3:14])([CH3:13])[CH3:12])=[O:9].C(N(CC)CC)C.[C:22]([O:26][C:27]([NH:29][C@H:30]1[C@H:33]([CH3:34])[NH:32][C:31]1=[O:35])=[O:28])([CH3:25])([CH3:24])[CH3:23]>C1(C)C=CC=CC=1.ClCCl.C(OCC)(=O)C>[C:22]([O:26][C:27]([NH:29][C@H:30]1[C@H:33]([CH3:34])[N:32]([C:31]([N:6]([CH3:5])[CH2:7][C:8]([O:10][C:11]([CH3:14])([CH3:13])[CH3:12])=[O:9])=[O:35])[C:1]1=[O:2])=[O:28])([CH3:25])([CH3:24])[CH3:23]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 4

HCID 6371PhosgeneHCID 8471Triethylamine3×HCID 5069406Tert-butyl 2-(methylamino)acetateHCID 13155285tert-Butyl ((2S,3S)-2-methyl-4-oxoazetidin-3-yl)carbamate

Produkt 1

HCID 131714548(3S-trans)-N-[[3-[[t-Butoxycarbonyl]amino]-4-methyl-2-oxo-1-azetidinyl]carbonyl]-N-methylglycine, t-butyl ester

Reagenzien, Katalysatoren, Lösungsmittel

3
HCID 1140TolueneLösungsmittelHCID 6344DichloromethaneLösungsmittel2×HCID 8857Ethyl AcetateLösungsmittel

Versuchsvorschrift

A solution of phosgene in toluene (1.35 ml of a 20% solution, 2.698 mmol) was cooled to -25° C. under an argon atmosphere. A solution of N-methylglycine, t-butyl ester (218 mg, 1.498 mmol) and triethylamine (251 μl, 1.798 mmol) in dichloromethane (2 ml) was added dropwise over 5 minutes. The reaction was stirred for 1 hour at -25° C. (after 15 minutes an additional 0.2 ml of dichloromethane was added to facilitate stirring). The volatiles were removed starting at -25° C. and slowly by warming to room temperature. The residue was dissolved in methylene chloride (5 ml), cooled to 0° C. and treated with (3S-trans)-3-[[t-butoxycarbonyl]amino]-4-methyl-2-azetidinone (300 mg, 1.498 mmol; pre-dried over P2O5 at 25° C. under high vacuum), 4-dimethylaminiopyridine (18 mg, 0.149 mmol), and triethylamine (251 μl, 1.798 mmol). The resulting mixture was warmed to room temperature, stirred for 36 hours, treated with additional triethylamine (502 μl), and refluxed for 5 hours. The reaction was cooled, diluted with ethyl acetate, washed with pH 4.5 KH2PO4, and with brine, and then dried over sodium sulfate. Filtration and concentration in vacuo produced 525 mg of an oil which was chromatographed on 21 g of silica gel (230-400 mesh). Elution with 40% ethyl acetate-hexane gave 356 mg of the title compound as a white solid.

Aufarbeitung

  1. additionwas added
  2. customThe volatiles were removed
  3. customstarting at -25° C.
  4. dissolutionThe residue was dissolved in methylene chloride (5 ml)
  5. temperaturecooled to 0° C.
  6. temperatureThe resulting mixture was warmed to room temperature
  7. stirringstirred for 36 hours
  8. temperaturerefluxed for 5 hours
  9. temperatureThe reaction was cooled
  10. washwashed with pH 4.5 KH2PO4
  11. dry with materialwith brine, and then dried over sodium sulfate
  12. filtrationFiltration and concentration in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-25da6eb50cac4975a77a2a733776fabe
Quelldatensatz
uspto-grants-1986_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04576749

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion