反応式
C1C=CC=CC=1.[F:7][C:8]1[C:9](=[O:42])[NH:10][C:11](=[O:41])[N:12]([CH:40]=1)[C@@H:13]1[O:39][C@H:17]([CH2:18][O:19]C(C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[C@@H:15]([OH:16])[CH2:14]1.[CH2:43](Br)[C:44]1[CH:49]=[CH:48][CH:47]=[CH:46][CH:45]=1.[OH-].[K+]>O1CCOCC1>[CH2:43]([O:16][C@@H:15]1[C@@H:17]([CH2:18][OH:19])[O:39][C@@H:13]([N:12]2[CH:40]=[C:8]([F:7])[C:9](=[O:42])[NH:10][C:11]2=[O:41])[CH2:14]1)[C:44]1[CH:49]=[CH:48][CH:47]=[CH:46][CH:45]=1参加物
実験手順
To a mixture of 50 ml of benzene and 50 ml of dioxane were added 1.00 g of 2'-deoxy-5-fluoro-5'-O-trityluridine, 0.30 ml of benzyl bromide and 0.23 g of potassium hydroxide powder, and the mixture was refluxed for 25 hours. The insolubles were removed by filtration and the filtrate was concentrated and the concentrate was dissolved in 5 ml of 80% acetic acid. The solution was left to stand at 80° C. for 2 hours. The solvent was distilled off and the residue was placed on a silica gel column to conduct a gradient elution using chloroform and mixtures of methanol (up to 2%) and chloroform. The fractions corresponding to 3'-O-benzyl-2'-deoxy-5-fluorouridine were collected and concentrated. The concentrate was recrystallized from ethanol, giving 0.14 g of the title compound in a yield of 20%.
後処理
- temperaturethe mixture was refluxed for 25 hours
- customThe insolubles were removed by filtration
- concentrationthe filtrate was concentrated
- dissolutionthe concentrate was dissolved in 5 ml of 80% acetic acid
- waitThe solution was left
- distillationThe solvent was distilled off
- washa gradient elution
- customThe fractions corresponding to 3'-O-benzyl-2'-deoxy-5-fluorouridine were collected
- concentrationconcentrated
- customThe concentrate was recrystallized from ethanol
出典と根拠
- ORDレコード
- ord-85b329a2a10f4a8388d5b30f839bd77c
- 出典データセット
- uspto-grants-1992_10
- 特許番号
- US05155113
関連ノート
読み込み中…