1,2,3,5-Tetraacetyl-beta-D-ribofuranose → 1-(2,3,5-Tri-O-acetyl-beta-D-ribofuranosyl)-1H-1,2,4-triazole-3-carbonitrile

HRID 1703732Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1703732
[C:1]([C:3]1[N:7]=[CH:6][NH:5][N:4]=1)#[N:2].C(O[C@@H:12]1[O:24][C@H:23]([CH2:25][O:26][C:27](=[O:29])[CH3:28])[C@@H:18]([O:19][C:20](=[O:22])[CH3:21])[C@H:13]1[O:14][C:15](=[O:17])[CH3:16])(=O)C.P([O-])(OC1C=CC([N+]([O-])=O)=CC=1)(OC1C=CC([N+]([O-])=O)=CC=1)=O>C(Cl)(Cl)Cl>[C:1]([C:3]1[N:7]=[CH:6][N:5]([C@@H:12]2[O:24][C@H:23]([CH2:25][O:26][C:27](=[O:29])[CH3:28])[C@@H:18]([O:19][C:20](=[O:22])[CH3:21])[C@H:13]2[O:14][C:15](=[O:17])[CH3:16])[N:4]=1)#[N:2]

Komponenten

5

Versuchsvorschrift

A mixture of 3-cyano-1,2,4-triazole (9.41 g., 0.10 mol) and 1,2,3,5-tetra-O-acetyl-β -D-ribofuranose (31.8 g., 0.10 mol) was heated in an oil bath maintained at 150°. Bis(p-nitrophenyl) phosphate (100 mg.) was added with stirring and heating at 150° under diminished pressure was continued for 15 min. The residue was dissolved in chloroform, the solution was filtered and the solvent was removed. Crystallization of the residue from ether provided 28.2 g. (80%) of product with M.P. 96-97°.

Aufarbeitung

  1. temperaturewas heated in an oil bath
  2. temperaturemaintained at 150°
  3. temperatureheating at 150° under diminished pressure
  4. filtrationthe solution was filtered
  5. customthe solvent was removed
  6. customCrystallization of the residue from ether
  7. customprovided 28.2 g

Quellen und Nachweise

ORD-Eintrag
ord-083541fcf06a4ad68edddddb140643e1
Quelldatensatz
uspto-grants-1978_11
Patentnummer
USRE029835

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