Formic Acid → N-(2-Chloroethyl)-N'-beta-D-glucopyranosyl-N-nitrosourea

HRID 263363

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HRID 263363 반응식
[NH2:1][C@@H:2]1[O:10][C@H:9]([CH2:11][OH:12])[C@@H:7]([OH:8])[C@H:5]([OH:6])[C@H:3]1[OH:4].C(O)=O.C(O)(=O)CC(CC(O)=O)(C(O)=O)O.[Cl:29][CH2:30][CH2:31][N:32]([N:45]=[O:46])[C:33](=O)[O:34]C1C=CC=CC=1[N+]([O-])=O>CO.O1CCOCC1.O1CCCC1>[C@@H:2]1([NH:1][C:33](=[O:34])[N:32]([CH2:31][CH2:30][Cl:29])[N:45]=[O:46])[O:10][C@H:9]([CH2:11][OH:12])[C@@H:7]([OH:8])[C@H:5]([OH:6])[C@H:3]1[OH:4]

참가 물질

8

실험 절차

1.79 g (10 mmol) of 1-amino-1-deoxy-β-D-glucopyranose is dissolved in a mixture of 20 ml methanol and 10 ml dioxane, and to this solution is added a mixture of formic acid and citric acid dropwise, with stirring, to adjust the PH of the solution to 9.1. The resulting solution is then added dropwise to a solution prepared by dissolving 3.28 g (12 mmol) of o-nitrophenyl N-(2-chloroethyl)-N-nitrosocarbamate in a mixture of 10 ml tetrahydrofuran and 15 ml dioxane, while stirring, at 5°-10° C. over 30 minutes. The resultant mixture is stirred at the same temperature for a further 4 hours, and the thus reacted solution is concentrated at 40° C. and below, under reduced pressure. The crystalline residue obtained is washed with anhydrous ethyl ether and then with acetone, dried under reduced pressure, and recrystallized from anhydrous ethanol-ethyl ether (4:1) to give 2.56 g of 3-(β-D-glucopyranosyl)-1-(2-chloroethyl)-1-nitrosourea. Yield 81.5%. mp 77°-78° C. (decomp.). [α]D25 -10.3° (C 1.0, water). Analysis for C9H16N3O7Cl (MW 313.69):

후처리

  1. additionto this solution is added
  2. additionThe resulting solution is then added dropwise to a solution
  3. customprepared
  4. stirringwhile stirring, at 5°-10° C. over 30 minutes
  5. concentrationthe thus reacted solution is concentrated at 40° C.
  6. customThe crystalline residue obtained
  7. washis washed with anhydrous ethyl ether
  8. dry with materialwith acetone, dried under reduced pressure
  9. customrecrystallized from anhydrous ethanol-ethyl ether (4:1)

출처 및 근거

ORD 기록
ord-9135feff2ddc457486749a511c3e74ee
출처 데이터셋
uspto-grants-1979_05
특허 번호
US04156777

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