Thionyl Chloride → 5-(Chloromethyl)uracil
反応式
S(Cl)([Cl:3])=O.O[CH2:6][C:7]1[C:8](=[O:14])[NH:9][C:10](=[O:13])[NH:11][CH:12]=1>O1CCOCC1>[Cl:3][CH2:6][C:7]1[C:8](=[O:14])[NH:9][C:10](=[O:13])[NH:11][CH:12]=1参加物
4
実験手順
Thionyl chloride ((10 ml) was added to a suspension of 5-(hydroxymethyl)-2,4(1H,3H)-pyrimidinedione (0.60 g, 4.2 mmol)from step (11a) in dioxane (15 ml). The reaction was heated to reflux for 4 h, allowed to cool, and concentrated in vacuo to give the 5-(chloromethyl)-2,4(1H,3H)-pyrimidinedione (0.62 g, 100%) as a yellow solid.
後処理
- temperatureThe reaction was heated
- temperatureto reflux for 4 h
- temperatureto cool
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-7ba52a75ba89449ebaa88639d2057de4
- 出典データセット
- uspto-grants-2006_09
- 特許番号
- US07101883B2
反応ノート
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