Carbon Dioxide → 2-[3-(2-Chloroethyl)-3-nitrosoureido]-D-glucopyranose

HRID 263359

Reaktionsgleichung

Reaktionsgleichung von HRID 263359
[NH2:1][C@@H:2]1[C@@H:8]([OH:9])[C@H:7]([OH:10])[C@@H:6]([CH2:11][OH:12])[O:5][CH:3]1[OH:4].C(=O)=[O:14].OC1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O.C(=O)(O)O.[Cl:32][CH2:33][CH2:34][N:35]([N:47]=[O:48])[C:36](=O)[O:37]C1C=CC=CC=1C#N>CO.CN(C)C=O.O1CCCC1.C(Cl)Cl>[OH:4][CH:3]1[O:5][C@H:6]([CH2:11][OH:12])[C@@H:7]([OH:10])[C@H:8]([OH:9])[C@@:2]1([NH:1][C:36](=[O:37])[N:35]([CH2:34][CH2:33][Cl:32])[N:47]=[O:48])[OH:14]

Komponenten

10

Versuchsvorschrift

1.79 g (10 mmol) of 2-amino-2-deoxy-D-glucopyranose is dissolved in a mixture of 20 ml anhydrous methanol and 10 ml dimethylformamide, and the solution is cooled to 0°-5° C. To this solution is added 2.2 g (50 mmol) of dry-ice little by little so as to convert said glucopyranose into its carbonic acid-addition salt. This acid-addition salt solution is then added dropwise to a solution prepared by dissolving 3.04 g (12 mmol) of o-cyanophenyl N-(2-chloroethyl)-N-nitrosocarbamate in a mixture of 20 ml anhydrous tetrahydrofuran and 10 ml methylene chloride, while stirring, at 0°-5° C. over an hour. The resultant mixture is stirred further at 22°-25° C. for 2 hours, and the thus reacted solution is concentrated at 40° C. and below, under reduced pressure. The crystalline residue obtained is washed with petroleum ether, dried under reduced pressure, and recrystallized from anhydrous ethanol to give 2.58 g of 3-(D-glucopyranos-2-yl)-1-(2-chloroethyl)-1-nitrosourea. Yield 82.2%. mp 147°-148° C. (decomp.). Analysis for C9H16N3O7Cl (MW 313.69):

Aufarbeitung

  1. temperaturethe solution is cooled to 0°-5° C
  2. additionThis acid-addition salt solution is then added dropwise to a solution
  3. customprepared
  4. concentrationthe thus reacted solution is concentrated at 40° C.
  5. customThe crystalline residue obtained
  6. washis washed with petroleum ether
  7. customdried under reduced pressure
  8. customrecrystallized from anhydrous ethanol

Quellen und Nachweise

ORD-Eintrag
ord-adf87f4c401845aaa4b2c56dd7adb21f
Quelldatensatz
uspto-grants-1979_05
Patentnummer
US04156777

Verknüpfte Notizen

Wird geladen…