반응 #5961

반응 방정식

2-amino-6-chloro-9-[2-(2,2-dimethyl-1,3-dioxan-5-yl)ethyl]purine

→

2-amino-9-(4-hydroxy-3-hydroxymethylbut-1-yl)purine

수율 36.1%

용매

ethanol

cyclohexene

반응 조건

후처리

1. 1
   온도the solution was refluxed for 7 hours
2. 2
   온도the solution was refluxed overnight
3. 3
   여과The solution was filtered
4. 4
   세척washed through with methanol
5. 5
   workup.ADDITIONTo the filtrate was added hydrochloric acid (5M, 0.3 ml) and water (0.7 ml)
6. 6
   workup.ADDITIONThe solution was neutralised by addition of aqueous sodium bicarbonate
7. 7
   기타the solvent was removed
8. 8
   기타The residue was purified by column chromatography on silica gel eluting with chloroform-methanol (5:1, 4:1)

실험 절차

To a solution of 2-amino-6-chloro-9-[2-(2,2-dimethyl-1,3-dioxan-5-yl)ethyl]purine (0.54 g, 1.75 mmol) in ethanol (10 ml) and cyclohexene (20 ml) was added 10% palladium-on-charcoal (400 mg) and the solution was refluxed for 7 hours. A further quantity of catalyst (200 mg) was added and the solution was refluxed overnight. The solution was filtered and washed through with methanol. To the filtrate was added hydrochloric acid (5M, 0.3 ml) and water (0.7 ml) and the solution was stirred for 30 minutes at room temperature. The solution was neutralised by addition of aqueous sodium bicarbonate and the solvent was removed. The residue was purified by column chromatography on silica gel eluting with chloroform-methanol (5:1, 4:1) to afford 2-amino-9-(4-hydroxy-3-hydroxymethylbut-1-yl)purine as a crystalline solid (150 mg, 36%), m.p. 156°-158° C.; λmax (H2O) 242 and 303 nm; λmax (KBr) 3320, 3210, 1640, 1610, 1580, and 1430 cm-1 ; δH [(CD3)2SO] 1.47 (1H, m, 3'-H), 1.78 (2H, q, J 7.2 Hz, 2'-H), 3.3-3.5 (4H, m, 2×4'-H), 4.12 (2H, t, J 7.4 Hz, 1'-H), 4.42 (2H, t, J 5.2 Hz, D2O exchangeable, 2×OH), 6.45 (2H, s, D2O exchangeable, 2-NH2), 8.06 (1H, s, 8-H), and 8.56 (1H, s, 6-H); (Found: C, 50.61; H, 6.45; N, 29.62%. C10H15N5O2 requires: C, 50.62; H, 6.37; N, 29.52%).

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