反応式
C([O:4][CH2:5][CH:6]([CH2:20][O:21]C(=O)C)[CH2:7][CH2:8][N:9]1[CH:17]=[N:16][C:15]2[C:10]1=[N:11][C:12]([NH2:19])=[N:13][C:14]=2Cl)(=O)C.C([O-])=O.[NH4+]>CO.[Pd]>[NH2:19][C:12]1[N:11]=[C:10]2[C:15]([N:16]=[CH:17][N:9]2[CH2:8][CH2:7][CH:6]([CH2:20][OH:21])[CH2:5][OH:4])=[CH:14][N:13]=1参加物
実験手順
To a suspension of 9-(4-acetoxy-3-acetoxymethylbut-1-yl)-2-amino-6-chloropurine (4.86 g, 13.7 mmol) in methanol (140 ml) containing ammonium formate (400 mM) was added 10% palladium-on-charcoal (0.4 g) and the mixture was heated under reflux for 40 minutes. After cooling the solution was filtered and the solvent removed. The residue was taken up in water and extracted with chloroform (100 ml and 50 ml). The organic layers were combined, dried (magnesium sulphate) and the solvent removed. The residue was dissolved in methanol saturated with ammonia at 0° C. (150 ml) and the solution was stirred for 20 hours. The solvent was removed and the residue suspended in chloroform (20 ml) and filtered. The solid was recrystallised from isopropanol-water and a second recrystallisation was carried out from the mother liquors from ethanol (total 2.71 g, 83%).
後処理
- temperaturethe mixture was heated
- temperatureunder reflux for 40 minutes
- temperatureAfter cooling the solution
- filtrationwas filtered
- customthe solvent removed
- extractionextracted with chloroform (100 ml and 50 ml)
- dry with materialdried (magnesium sulphate)
- customthe solvent removed
- dissolutionThe residue was dissolved in methanol saturated with ammonia at 0° C. (150 ml)
- customThe solvent was removed
- filtrationfiltered
- customThe solid was recrystallised from isopropanol-water
- customa second recrystallisation
出典と根拠
- ORDレコード
- ord-9a26110b23a143e0bf216102d09220cd
- 出典データセット
- uspto-grants-1993_09
- 特許番号
- US05246937
関連ノート
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