Adenine → 9-(Phenylmethyl)-9H-purin-6-amine
反応式
[N:1]1[C:9]([NH2:10])=[C:8]2[C:4]([N:5]=[CH:6][NH:7]2)=[N:3][CH:2]=1.[H-].[Na+].[CH2:13](Br)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1>CN(C=O)C>[CH2:13]([N:5]1[CH:6]=[N:7][C:8]2[C:4]1=[N:3][CH:2]=[N:1][C:9]=2[NH2:10])[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1参加物
5
反応条件
- 温度
- 100 °C
実験手順
Adenine (1 mmol) in DMF was treated with sodium hydride (1.2 mmol) followed by benzyl bromide (1.2 mmol) at room temperature under nitrogen. The resulting mixture was warmed at 100° C. for 2 h. The cooled reaction mixture was evaporated to dryness. Extraction and chromatography afforded N9-benzyladenine.
後処理
- customThe cooled reaction mixture
- customwas evaporated to dryness
- extractionExtraction and chromatography
出典と根拠
- ORDレコード
- ord-a631dcfe8f3941e3912af92044a6d41c
- 出典データセット
- uspto-grants-2007_10
- 特許番号
- US07285543B2
反応ノート
読み込み中…