반응 #710509

ord-08be6ac03d714254b0303bbc09bd48d8

반응 방정식

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

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    여과filtering the resultant
  2. 2
    기타to remove palladium carbon
  3. 3
    기타drying the resulting solution in vacuo
  4. 4
    workup.ADDITIONadding ethanol
  5. 5
    여과filtering the resultant
  6. 6
    기타to obtain a crude crystalline adenosine N1-oxide
  7. 7
    workup.DISSOLUTIONThe crude crystals were dissolved
  8. 8
    여과filtered
  9. 9
    온도ice chilled for crystallization
  10. 10
    기타the recrystallization step twice

실험 절차

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%.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09301968B2uspto-grants-2016_04