HRID566697

反应详情

EQUATION

反应方程式

HRID 566697 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

2′-deoxy-2-fluoroadenosine (20, 12 g, 0.45 mol) and dimethoxytrityl chloride (18.1 g, 0.53 mol) were dissolved in anhydrous pyridine (100 mL) and stirred at ambient temperature until the trace amount of the starting material remaining matched the bis DMT impurity forming (3 h) as monitored by TLC (Rf 0.20, starting material; Rf 0.60, product; Rf 0.85, bis DMT product, ethyl acetate-methanol 9:1). The reaction was quenched by the addition of methanol (50 mL) and then concentrated under reduced pressure to an oil. The residue was partitioned between ethyl acetate (250 mL) and sat'd sodium bicarbonate (250 mL). The aqueous layer was extracted with ethyl acetate (100 mL) once more and the combined extracts were concentrated under reduced pressure. The resulting oil was purified by silica gel chromatography (400 g) using a gradient of methanol in ethyl acetate (0-5%). The appropriate fractions were combined, concentrated under reduced pressure, coevaporated with anhydrous acetonitrile (200 mL) and dried (1 mm Hg, 25° C., 24 h) to a foam, 23.2 g (90%). The product can be crystallized from dichloromethane to give white crystals, mp 239-243° C. H-NMR (DMSO-d6) d 2.2-2.4 and 2.7-2.9 (m, 2, 2′-CH2), 3.18 (m, 2, 5′-H and 5″-H), 3.75 (s, 6, O—CH3), 3.98 (m, 1, 4′-H), 4.43 (m, 1, 3′-H), 5.38 (d, 1, 3′-OH), 6.15 (t, 1, 1′-H), 6.83 (m, 4, arom.), 7.15-7.4 (m, 9, arom.), 7.83 (br s, 2, NH2), 8.23 (s, 1, 8-H). F-NMR (DMSO-d6) δ-53.5 (s).

WORKUP

后处理

  1. customforming (3 h)
  2. customThe reaction was quenched by the addition of methanol (50 mL)
  3. concentrationconcentrated under reduced pressure to an oil
  4. customThe residue was partitioned between ethyl acetate (250 mL) and sat'd sodium bicarbonate (250 mL)
  5. extractionThe aqueous layer was extracted with ethyl acetate (100 mL) once more
  6. concentrationthe combined extracts were concentrated under reduced pressure
  7. customThe resulting oil was purified by silica gel chromatography (400 g)
  8. concentrationconcentrated under reduced pressure
  9. customdried (1 mm Hg, 25° C., 24 h) to a foam, 23.2 g (90%)
  10. customThe product can be crystallized from dichloromethane
  11. customto give white crystals, mp 239-243° C