反応式
Cl[C:2]1[CH:7]=[N:6][C:5]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)=[CH:4][N:3]=1.N1C=CC=CC=1.O.[NH2:21][NH2:22]>O>[NH:21]([C:2]1[CH:7]=[N:6][C:5]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)=[CH:4][N:3]=1)[NH2:22]参加物
5
実験手順
A mixture of 1.0 g. of 2-chloro-5-phenylpyrazine, m.p. 98°-99° C., 5.0 ml. of pyridine and 5.0 ml. of hydrazine hydrate is heated at reflux for 1.5 hours. The solution is cooled, and 20 ml. of water is added. The colorless crystalline product is collected and air dried. The crude product is recrystallized from aqueous ethanol to yield 0.35 g. of the product of the example as colorless needles, m.p. 128°-130° C.
後処理
- additionA mixture of 1.0 g
- temperatureat reflux for 1.5 hours
- temperatureThe solution is cooled
- customThe colorless crystalline product is collected
- customair dried
- customThe crude product is recrystallized from aqueous ethanol
- customto yield 0.35 g
出典と根拠
- ORDレコード
- ord-21ffbdf0805c4b64b5feca5098d9f0ce
- 出典データセット
- uspto-grants-1983_09
- 特許番号
- US04402958
関連ノート
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