تفاعل #51517

ord-30d4dc67ffcc47cfbdd9fa717f792f80

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىover 10 minutes
  2. 2
    workup.WAITleft
  3. 3
    workup.WAITto stand for 8 hours
  4. 4
    أخرىto give a gum
  5. 5
    أخرىThe solvent was decanted
  6. 6
    أخرىevaporated in vacuo
  7. 7
    أخرىto afford a white solid which
  8. 8
    استخلاصthis solution was gently extracted with the CH2Cl2 containing the product
  9. 9
    أخرىThe organic layer was separated
  10. 10
    استخلاصthe aqueous layer was extracted again with CH2Cl2 (2×50 mL)
  11. 11
    تجفيفthe solvent was dried over MgSO4
  12. 12
    أخرىevaporated in vacuo
  13. 13
    أخرىto afford a white foam
  14. 14
    أخرىpurified by flash chromatography

الإجراء التجريبي

1-[2′-O-(2-Ethylacetyl)-3′,5′-bis-O-(2,4-dichlorobenzyl)-β-D-ribofuranosyl]thymine (9.92 g, 15.0 mmol) was dissolved in hot EtOH (150 mL) and the solution was cooled to ambient temperature in a water bath. To the solution was cautiously added NaBH4 (1.13 g, 30.0 mmol) over 10 minutes. After 3 hours additional NaBH4 (282 mg, 7.45 mmol) was added the mixture was stirred for 1 hour and left to stand for 8 hours. The pH was adjusted to 4 by addition of Saturated NH4Cl (25 mL) to give a gum. The solvent was decanted and evaporated in vacuo to afford a white solid which was dissolved in CH2Cl2 (250 mL). The gum was dissolved with saturated aqueous NaHCO3 and this solution was gently extracted with the CH2Cl2 containing the product. The organic layer was separated and the aqueous layer was extracted again with CH2Cl2 (2×50 mL). After combining the organic layers, the solvent was dried over MgSO4 and evaporated in vacuo to afford a white foam. The foam was dissolved in CH2Cl2 and purified by flash chromatography using hexanes-EtOAc, 20:80, to give the title compound as a white foam (8.39 g, 90%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06849723B2uspto-grants-2005_02