Thymidine → HCID 67703974, compound

HRID 1376453Notes

Reaction equation

HRID 1376453 reaction equation
C(N([C:6]1[N:14]=[C:13]2[C:9]([N:10]=[CH:11][NH:12]2)=[CH:8][N:7]=1)CC)C.[F:15][C@@H:16]1[C@@H:20]([CH2:21][OH:22])[O:19][C@@H:18](N2C=CC(=O)NC2=O)[CH2:17]1.[N-]=[N+]=[N-].[K+].[C@@H:35]1([N:43]2[CH:51]=[C:49](C)C(=O)NC2=O)O[C@H](CO)[C@@H](O)[CH2:36]1>P([O-])([O-])([O-])=O.[K+].[K+].[K+].CO>[F:15][C@@H:16]1[C@@H:20]([CH2:21][OH:22])[O:19][C@@H:18]([N:12]2[CH:11]=[N:10][C:9]3[C:13]2=[N:14][CH:6]=[N:7][C:8]=3[N:43]([CH2:51][CH3:49])[CH2:35][CH3:36])[CH2:17]1

Participants

7

Reactant 4

HCID 5789ThymidineHCID 1624502',3'-Dideoxy-3'-fluorouridineHCID 10290740Potassium azideHCID 178463875HCID 178463875, compound

Product 1

HCID 67703974HCID 67703974, compoundYield 46%

Reagents, catalysts & solvents 2

HCID 887MethanolSolventHCID 62657Potassium Phosphate, TribasicSolvent

Conditions

Temperature
45 °C

Procedure

6 Diethylamino-9H-purine (0.50 g, 2.6 mmoles) and 2',3'-dideoxy-3'-fluorouridine (0.72 g, 3.2 mmoles) were suspended in 50 ml, 10 mM potassium phosphate buffer, pH 7.0, containing 0.04% potassium azide. Purine nucleoside phosphorylase (1120 I.U.) and thymidine phosphorylase (10,000 I.U.) (Krenitsky et al., Biochemistry, 20, 3615 (1981) and U.S. Pat. No. 4,381,344) immobilized on DEAE cellulose was added to the reaction and the suspension was stirred at 45° C. After 11 days, 150 ml MeOH was added to the reaction. The reaction was applied to a column containing AG1-X2 (OH-- form, 2.5×10 cm) and eluted with MeOH. Fractions containing product were pooled, concentrated, and flash chromatographed on silica gel (2.5×20 cm) with dichloromethane:acetone (9:1). Solvent was removed and lyophilization yielded 0.372 g of 9-(2,3-dideoxy-3-fluoro-β-D-erythro-pentofuranosyl)-6-diethylamino-9H-purine (46%): mp 114°-115° C.; TLC Rf 0.70 (silica gel, MeCN:15N NH4OH:H2O/85:5:10);

Workup

  1. additionwas added to the reaction
  2. additioncontaining AG1-X2 (OH-- form, 2.5×10 cm)
  3. washeluted with MeOH
  4. additionFractions containing product
  5. concentrationconcentrated
  6. customflash chromatographed on silica gel (2.5×20 cm) with dichloromethane:acetone (9:1)
  7. customSolvent was removed

Sources & evidence

ORD record
ord-6d8314409c73401eb3585c2c3d1be76f
Source dataset
uspto-grants-1997_09
Patent number
US05663154

Reaction notes

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