Thymidine → HCID 67703960, compound

HRID 1376461Notes

Reaction equation

HRID 1376461 reaction equation
[NH:1]([C:8]1[N:16]=[CH:15][N:14]=[C:13]2[C:9]=1[N:10]=[CH:11][NH:12]2)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[F:17][C@@H:18]1[C@@H:22]([CH2:23][OH:24])[O:21][C@@H:20](N2C=CC(=O)NC2=O)[CH2:19]1.[N-]=[N+]=[N-].[K+].[C@@H]1(N2C=C(C)C(=O)NC2=O)O[C@H](CO)[C@@H](O)C1>P([O-])([O-])([O-])=O.[K+].[K+].[K+].CO>[NH:1]([C:8]1[N:16]=[CH:15][N:14]=[C:13]2[C:9]=1[N:10]=[CH:11][N:12]2[C@@H:20]1[O:21][C@H:22]([CH2:23][OH:24])[C@@H:18]([F:17])[CH2:19]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Participants

7

Reactant 4

HCID 5789ThymidineHCID 1624502',3'-Dideoxy-3'-fluorouridineHCID 10290740Potassium azideHCID 178420486HCID 178420486, compound

Product 1

HCID 67703960HCID 67703960, compoundYield 45%

Reagents, catalysts & solvents 2

HCID 887MethanolSolventHCID 62657Potassium Phosphate, TribasicSolvent

Conditions

Temperature
45 °C

Procedure

6-Anilino-9H-purine (0.55 g 2.6 mmoles) and 2',3'-dideoxy-3'-fluorouridine (0.50 g, 2.2 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 4 days, 180 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 (93:7). Solvent was removed and lyophilization yielded 0.323 g of 6-anilino-9-(2,3-dideoxy-3-fluoro-β-D-erythro-pentofuranosyl)-9H-purine (45%): mp 83° C.; TLC Rf 0.72 (silica gel, MeCN:15N NH4OHiH2O/85:5:10); [α]D20 -18.8 (c=0.5, DMF); UV λmax (ε×10-3) at pH 7,288 (22.2); at pH 13, 288 (21.0); 1H NMR (300 MHz, DMSO-d6) δ9.98 (s, 1H, NH), 8.54 and 8.41 (2s, 2H, H2 and H8), 7.95 (d, 2H, J=7.6 Hz), 7.31-7.37 (m, 2H), 7.06 (t, 1H, J=7.4 Hz), 6.48 (dd, 1H, H1', J=9.2 Hz, J=5.7 Hz), 5.38-5.58 (m, 2H, OH5' and H3'), 4.28 (dt, 1H, H4', J=26.8 Hz, J=4.6 Hz) 3.65 (m, 2H, H5' and H5"), and 2.97-3.18 and 2.64-2.78 (m, 2H, H2' and H2"); MS (ci) 330 (M+1), 310 (M-F), 212 (MH2 --C5H8FO2).

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 (93:7)
  7. customSolvent was removed

Sources & evidence

ORD record
ord-ac48a19fcd1743a08f0c7e4c65986736
Source dataset
uspto-grants-1997_09
Patent number
US05663154

Reaction notes

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