반응 #49780

ord-07024dfe133a492982eb346fb71788a5

반응 조건

온도
35°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITION4,381,344) were added
  2. 2
    여과Twenty days later the reaction was filtered
  3. 3
    기타the filtrate chromatographed on a column
  4. 4
    workup.ADDITIONcontaining Dowex-1-hydroxide resin (2.5×8 cm)
  5. 5
    세척The product was eluted from the column with 90% methanol/water (v/v)
  6. 6
    workup.ADDITIONFractions containing product
  7. 7
    기타the solvent removed under vacuum
  8. 8
    workup.DISSOLUTIONThe residue was dissolved in 50 ml of 30% n-propanol
  9. 9
    기타water (v/v) and chromatographed on a BioRad P-2 column (5×90 cm)
  10. 10
    세척The product was eluted with 30% n-propanol/water (v/v)
  11. 11
    기타the solvent was removed under vacuum

실험 절차

6-Pyrrolidinopurine (Sigma Chemical Co., St. Louis, Mo.) (2.6 mmoles), 0.5 g, and uracil arabinoside (5.29 mmoles, 1.29 g) were suspended in 100 ml of a 10 mM potassium phosphate 0.04% potassium azide solution with a pH of 7.4. Purified uridine phosphorylase (6000 I.U.) and purine nucleoside phosphorylase (8400 I.U.) (Krenitsky, T. A., et al. Biochemistry, 20, 3615 (1981) and U.S. Pat. No. 4,381,344) were added and the suspension stirred at 35° C. Twenty days later the reaction was filtered and the filtrate chromatographed on a column containing Dowex-1-hydroxide resin (2.5×8 cm). The product was eluted from the column with 90% methanol/water (v/v). Fractions containing product were combined and the solvent removed under vacuum. The residue was dissolved in 50 ml of 30% n-propanol and water (v/v) and chromatographed on a BioRad P-2 column (5×90 cm). The product was eluted with 30% n-propanol/water (v/v). Product-containing fractions were combined and the solvent was removed under vacuum yielding 0.573 g of 9-β-D-arabinofuranosyl-6-pyrrolidino-9H-purine. NMR and mass spectrometry were consistent with the structure. Anal. Calcd. for C14H19N5O4 : Calcd: C, 52.33; H, 5.96 N, 21.79. Found: C, 52.60; H, 6.09; N, 21.51.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05424295uspto-grants-1995_06