反応式
[NH2:1][C:2]1[NH:6][N:5]=[C:4]([CH2:7][OH:8])[N:3]=1.[CH3:9][C:10](=O)[CH2:11][C:12](=O)[CH3:13]>C(O)(=O)C>[CH3:9][C:10]1[CH:11]=[C:12]([CH3:13])[N:6]2[N:5]=[C:4]([CH2:7][OH:8])[N:3]=[C:2]2[N:1]=1参加物
4
実験手順
To a slurry of (5-amino-1H-[1,2,4]triazol-3-yl)-methanol (9.5 g, 50 mmol) from Step 1 above in acetic acid (200 mL) was added 2,4-pentanedione (5.13 mL, 50 mmol). The mixture was heated to reflux for 4 hours, and then cooled to room temperature. The product was isolated by removing the solvent by rotary evaporation (8.5 g, 95% yield).
後処理
- temperatureThe mixture was heated
- temperatureto reflux for 4 hours
- customThe product was isolated
- customby removing the solvent
- customby rotary evaporation (8.5 g, 95% yield)
出典と根拠
- ORDレコード
- ord-c8aa1bff22ac42d4aa2e41ab42ebebef
- 出典データセット
- uspto-grants-2006_12
- 特許番号
- US07148226B2
関連ノート
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