Sodium → Doxifluridine

HRID 1759378

反応式

HRID 1759378 の反応式
C([O:4][C@@H:5]1[C@H:9]([O:10]C(=O)C)[C@@H:8]([CH3:14])[O:7][C@H:6]1[N:15]1[CH:22]=[C:21]([F:23])[C:19](=[O:20])[NH:18][C:16]1=[O:17])(=O)C.C[O-].[Na+].[Na]>CO>[F:23][C:21]1[C:19](=[O:20])[NH:18][C:16](=[O:17])[N:15]([CH:22]=1)[C@@H:6]1[O:7][C@H:8]([CH3:14])[C@@H:9]([OH:10])[C@H:5]1[OH:4]

参加物

5

反応条件

温度
0 °C

実験手順

A solution of 860 g of 1-(5-deoxy-2,3-di-O-acetyl-β-D-ribofuranosyl)-5-fluorouracil in 16 liters of methanol was added to sodium methoxide freshly prepared from 42 g of sodium and 2000 ml of methanol. The methyl acetate resulting during the reaction was removed by repeated concentration of the mixture. The mixture was neutralised by the addition of 1000 ml of a strongly acidic cation exchange resin (H+ -form), freshly washed with methanol. After removing the ion exchange resin, the methanolic solution was concentrated under reduced pressure and the product, which separated in crystalline form, was washed with a mixture, cooled to 0° C., of 1000 ml of methanol and 1000 ml of ethyl acetate. By working-up the mother liquors there was obtained a total of 680 g (97%) of pure 5'-deoxy-5-fluorouridine; m.p. 192°-193° C.; [β]D25 =+139° (c=0.9 in methanol).

後処理

  1. customThe methyl acetate resulting during the reaction was removed
  2. additionThe mixture was neutralised by the addition of 1000 ml of a strongly acidic cation exchange resin (H+ -form)
  3. washfreshly washed with methanol
  4. customAfter removing the ion exchange resin
  5. concentrationthe methanolic solution was concentrated under reduced pressure
  6. customthe product, which separated in crystalline form
  7. washwas washed with a mixture

出典と根拠

ORDレコード
ord-a5847a422c334566bef67fa7ec849c2d
出典データセット
uspto-grants-1982_07
特許番号
US04340729

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