methyl 2-deoxy-2-fluoro-alpha-D-ribofuranoside → GlyTouCan:G23553KL

HRID 965384ノート

反応式

HRID 965384 の反応式
[F:1][C@@H:2]1[C@H:8]([OH:9])[C@@H:7]([CH2:10][OH:11])[O:6][C@@H:3]1[O:4]C.F[C@@H]1[C@H](O)[C@@H](CO)O[C@H:14]1[O:15]C>>[F:1][C@@H:2]1[C@H:8]([OH:9])[C@@H:7]([CH2:10][OH:11])[O:6][CH:3]([OH:4])[C@@H:14]1[OH:15]

参加物

3

実験手順

The mixture of compounds (4) and (5) obtained in item (2) above (10.0 g) was dissolved in pyridine (200 ml), to which benzoyl chloride (17.5 ml) was then added, and the resulting mixture was allowed to stand at room temperature for 30 minutes. After addition of a small amount of water, the resultant reaction solution was concentrated, and the syrup obtained was extracted with chloroform. The solution in chloroform was washed with a 5% aqueous potassium hydrogen sulfate solution, a 5% aqueous sodium hydrogen carbonate solution and water, successively, and then dried over anhydrous sodium sulfate and concentrated to afford a mixture of the titled compounds (6) and (7) (22.3 g) as colorless crystals. Yield: 99%.

出典と根拠

ORDレコード
ord-cfbdddba69e14b199404b37aa6e9dbd2
出典データセット
uspto-grants-1998_06
特許番号
US05773607

反応ノート

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