Butylamine → N2-butyl-9H-purine-2,6-diamine
反応式
Cl[C:2]1[N:10]=[C:9]2[C:5]([NH:6][CH:7]=[N:8]2)=[C:4]([NH2:11])[N:3]=1.[CH2:12]([NH2:16])[CH2:13][CH2:14][CH3:15]>>[CH2:12]([NH:16][C:2]1[N:10]=[C:9]2[C:5]([NH:6][CH:7]=[N:8]2)=[C:4]([NH2:11])[N:3]=1)[CH2:13][CH2:14][CH3:15]参加物
3
実験手順
2-Chloroadenine (6.0 g, 35.4 mmol) and n-butylamine (30 ml) were reacted in an autoclave (200 ml) at 130° C. for 150 hours. After the reaction mixture was concentrated under reduced pressure, the residue was poured into water to precipitate the solid. The precipitated solid was successively washed with methylene chloride and methanol to give the captioned compound (2.08 g, yield 30%) as a yellowish orange powdered solid.
後処理
- concentrationAfter the reaction mixture was concentrated under reduced pressure
- additionthe residue was poured into water
- customto precipitate the solid
- washThe precipitated solid was successively washed with methylene chloride and methanol
出典と根拠
- ORDレコード
- ord-debc8edaefc5438b977e7327af820497
- 出典データセット
- uspto-grants-2010_07
- 特許番号
- US07754728B2
反応ノート
読み込み中…