Methanol → HCID 18396724, Verbindung

HRID 2289390Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2289390
[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-28348a6d89874e98bdaeb9d72e40643f
Quelldatensatz
uspto-grants-2000_07
Patentnummer
US06093412

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