9-(Phenylmethyl)-9H-purin-6-amine → 9-Benzyl-8-bromoadenine
反応式
[CH2:1]([N:8]1[CH:16]=[N:15][C:14]2[C:9]1=[N:10][CH:11]=[N:12][C:13]=2[NH2:17])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Br:18]Br>C(O)(=O)C>[CH2:1]([N:8]1[C:16]([Br:18])=[N:15][C:14]2[C:9]1=[N:10][CH:11]=[N:12][C:13]=2[NH2:17])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1参加物
4
実験手順
A solution of N9-benzyladenine (1 mmol) in acetic acid buffer (pH=4) was treated with bromine (1 mmol) at room temperature for 12 h. The reaction was quenched with 10% sodium sulfite solution and extracted with dichloromethane. The combined extracts were dried (Na2SO4) and evaporated to dryness. Chromatography afforded N9-benzyl-8-bromoadenine.
後処理
- customThe reaction was quenched with 10% sodium sulfite solution
- extractionextracted with dichloromethane
- dry with materialThe combined extracts were dried (Na2SO4)
- customevaporated to dryness
出典と根拠
- ORDレコード
- ord-2db62fd8c0334adb8d7276fe781e2b17
- 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…