Réaction #710509

ord-08be6ac03d714254b0303bbc09bd48d8

Équation de réaction

Nc1ncnc2c1ncn2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
adenosine
OO
hydrogen peroxide
OO
hydrogen peroxide
Nc1c2ncn([C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O)c2nc[n+]1[O-]
adenosine N1-oxide

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Filtrationfiltering the resultant
  2. 2
    Autreto remove palladium carbon
  3. 3
    Autredrying the resulting solution in vacuo
  4. 4
    workup.ADDITIONadding ethanol
  5. 5
    Filtrationfiltering the resultant
  6. 6
    Autreto obtain a crude crystalline adenosine N1-oxide
  7. 7
    workup.DISSOLUTIONThe crude crystals were dissolved
  8. 8
    Filtrationfiltered
  9. 9
    Températureice chilled for crystallization
  10. 10
    Autrethe recrystallization step twice

Mode opératoire

Twenty grams of adenosine (commercialized by Sigma-Aldrich Corporation, St. Louis, Mo. USA, Product code: A9251-25G) was dispersed in one liter of acetic acid, admixed with 100 mL of hydrogen peroxide solution, and stirred at ambient temperature for five days. To the resulting solution was added five grams of 5% palladium on carbon, commercialized by Kawaken Fine Chemicals Co., Ltd, Tokyo, Japan, followed by decomposing an excessive amount of hydrogen peroxide, filtering the resultant to remove palladium carbon, drying the resulting solution in vacuo, adding ethanol to unstiffen the formed crystals, and filtering the resultant to obtain a crude crystalline adenosine N1-oxide. The crude crystals were dissolved by heating in two liters of ethanol, filtered, and ice chilled for crystallization, followed by repeating the recrystallization step twice to obtain eight grams of adenosine N1-oxide with a purity of 99.5%.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09301968B2uspto-grants-2016_04