Methanol → HCID 18396724, Verbindung

HRID 848931Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 848931
[CH2:1]([NH:13][C:14]([N:16]1[CH:20]=[CH:19]N=[CH:17]1)=[O:15])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12].CNC[C@@H:24]([C@H:26]([C@@H:28]([C@@H:30](CO)[OH:31])[OH:29])[OH:27])[OH:25].C[OH:35]>>[CH2:1]([NH:13][C:14]([N:16]([CH3:17])[CH2:20][C@@H:19]([C@H:24]([C@@H:26]([C@@H:28]([CH2:30][OH:31])[OH:29])[OH:27])[OH:25])[OH:35])=[O:15])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12]

Komponenten

4

Versuchsvorschrift

42 g of 1-N-(dodecylaminocarbonyl)imidazole and 32 g of N-methyl-D-glucamine were suspended, under an inert atmosphere, in 400 cm3 of methanol. The reaction mixture was kept stirring at reflux for 4 hours. The reaction mixture was cooled with an ice bath and the precipitate was then filtered off. It was washed with 500 cm3 of water and then dried. 49 g (80% yield) of N-dodecylaminocarbonyl-N-methyl-D-glucamine were obtained in the form of a white powder.

Aufarbeitung

  1. temperatureat reflux for 4 hours
  2. temperatureThe reaction mixture was cooled with an ice bath
  3. filtrationthe precipitate was then filtered off
  4. washIt was washed with 500 cm3 of water
  5. customdried

Quellen und Nachweise

ORD-Eintrag
ord-1187477f8c534cdfbd1360f57359892e
Quelldatensatz
uspto-grants-2000_01
Patentnummer
US06010707

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