反応式
[C:1]([C:3]1[CH:8]=[CH:7][N:6]=[CH:5][CH:4]=1)#[N:2].[OH2:9]>O1CCCC1>[N:6]1[CH:7]=[CH:8][C:3]([C:1]([NH2:2])=[O:9])=[CH:4][CH:5]=1参加物
4
実験手順
(0.0051 g, 0.0119 mmol) of the platinum complex, prepared as in Example 1, was stirred with 4-cyanopyridine (2.0 g, 0.019 mol) and 0.75 ml (0.042 mol) of water and 10 ml tetrahydrofuran and the mixture heated under reflux for 4 hours. After cooling the liquids were removed using a rotary evaporator to give pyridine 4-carboxamide (2.12 g) corresponding to 90% yield.
後処理
- custom(0.0051 g, 0.0119 mmol) of the platinum complex, prepared as in Example 1
- temperaturethe mixture heated
- temperatureunder reflux for 4 hours
- temperatureAfter cooling the liquids
- customwere removed
- customa rotary evaporator
出典と根拠
- ORDレコード
- ord-abe4130096944c17b8c663f5db1a3233
- 出典データセット
- uspto-grants-2000_10
- 特許番号
- US06133478
関連ノート
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