Water → 5'-O-(Bis(4-methoxyphenyl)(phenyl)methyl)-2'-deoxy-2'-fluorouridine

HRID 84063ノート

反応式

HRID 84063 の反応式
[F:1][C@@H:2]1[C@H:6]([OH:7])[C@@H:5]([CH2:8][OH:9])[O:4][C@H:3]1[N:10]1[CH:17]=[CH:16][C:14](=[O:15])[NH:13][C:11]1=[O:12].[CH3:18][O:19][C:20]1[CH:41]=[CH:40][C:23]([C:24](Cl)([C:33]2[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=2)[C:25]2[CH:30]=[CH:29][C:28]([O:31][CH3:32])=[CH:27][CH:26]=2)=[CH:22][CH:21]=1.C(OCC)(=O)C.O>N1C=CC=CC=1>[CH3:32][O:31][C:28]1[CH:27]=[CH:26][C:25]([C:24]([O:9][CH2:8][C@H:5]2[O:4][C@@H:3]([N:10]3[CH:17]=[CH:16][C:14](=[O:15])[NH:13][C:11]3=[O:12])[C@H:2]([F:1])[C@@H:6]2[OH:7])([C:33]2[CH:34]=[CH:35][CH:36]=[CH:37][CH:38]=2)[C:23]2[CH:40]=[CH:41][C:20]([O:19][CH3:18])=[CH:21][CH:22]=2)=[CH:30][CH:29]=1

参加物

6

反応物 4

HCID 962WaterHCID 8857Ethyl AcetateHCID 968311,1'-(Chlorophenylmethylene)bis(4-methoxybenzene)HCID 1508512'Fluoro-2'-deoxyuridine

生成物 1

HCID 70731865'-O-(Bis(4-methoxyphenyl)(phenyl)methyl)-2'-deoxy-2'-fluorouridine収率 126.7%

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

実験手順

An operation of dissolving 2′-Deoxy-2′-fluorouridine (3.00 g, 12.2 mmol) in dry pyridine, followed by concentration under reduced pressure was repeated 3 times to perform dehydrative azeotropic distillation. Thereafter, under an argon atmosphere, the reaction mixture was dissolved in dry pyridine (120 ml), 4,4′-dimethoxytrityl chloride (4.55 g, 13.4 mmol) was added, and the mixture was stirred at room temperature for 3 hr. The completion of the reaction was confirmed, and ethyl acetate (150 ml) and water (60 ml) were added to the reaction mixture to allow layer separation. The organic layer was washed 3 times with 5% aqueous sodium hydrogen carbonate solution (20 ml), washed with water (20 ml) and saturated brine (20 ml), and the obtained organic layer was dried over sodium sulfate. The solvent in the filtrate was evaporated and the obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate=50:50-0/100 (v/v), containing 1% triethylamine). The object fractions were collected and concentrated to give the title compound (8.48 g, quant).

後処理

  1. distillationazeotropic distillation
  2. dissolutionThereafter, under an argon atmosphere, the reaction mixture was dissolved in dry pyridine (120 ml)
  3. customlayer separation
  4. washThe organic layer was washed 3 times with 5% aqueous sodium hydrogen carbonate solution (20 ml)
  5. washwashed with water (20 ml) and saturated brine (20 ml)
  6. dry with materialthe obtained organic layer was dried over sodium sulfate
  7. customThe solvent in the filtrate was evaporated
  8. customthe obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate=50:50-0/100 (v/v), containing 1% triethylamine)
  9. customThe object fractions were collected
  10. concentrationconcentrated

出典と根拠

ORDレコード
ord-40e4a7d6907d4433a85732a382139631
出典データセット
uspto-grants-2014_09
特許番号
US08846885B2

反応ノート

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