Hydrochloric Acid → 5-(4-Aminophenyl)pyrazin-2(1H)-one

HRID 542458

反応式

HRID 542458 の反応式
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10]2[N:11]=[CH:12][C:13](=[O:16])[NH:14][CH:15]=2)=[CH:6][CH:5]=1)([O-])=O.O.NN.O.Cl>C(O)C.[Pd]>[NH2:1][C:4]1[CH:5]=[CH:6][C:7]([C:10]2[N:11]=[CH:12][C:13](=[O:16])[NH:14][CH:15]=2)=[CH:8][CH:9]=1

参加物

7

反応物 4

HCID 313Hydrochloric AcidHCID 962Water3 回HCID 24654Hydrazine hydrate (1:1)HCID 138535735-(4-Nitrophenyl)pyrazin-2(1H)-one

生成物 1

HCID 123580285-(4-Aminophenyl)pyrazin-2(1H)-one収率 69.6%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 702Ethanol溶媒

実験手順

5-(4-Nitrophenyl)-2-(1H)-pyrazinone (0.1 g) was warmed with hydrazine hydrate (1 ml) in 50% aqueous ethanol (2.5 ml). Water (about 3 ml) was added sufficient to provide a clear solution. The mixture was allowed to cool slightly and 10% Palladium on charcoal (0.01 g) added as a slurry in a small amount of water. The well-stirred mixture was re-heated for 2 minutes, stirred without heating for 2 minutes, cooled and filtered. The filtrate was evaporated under reduced pressure to give a residue which was suspended in a little water. Dilute hydrochloric acid was added to pH6; the pale yellow solid was collected and washed with water to afford 5-(4-aminophenyl)-2(1H)-pyrazinone (0.06 g).

後処理

  1. customto provide a clear solution
  2. temperatureto cool slightly
  3. temperatureThe well-stirred mixture was re-heated for 2 minutes
  4. temperaturewithout heating for 2 minutes
  5. temperaturecooled
  6. filtrationfiltered
  7. customThe filtrate was evaporated under reduced pressure
  8. customto give a residue which
  9. customthe pale yellow solid was collected
  10. washwashed with water

出典と根拠

ORDレコード
ord-2945595124be4f9aa30c47a2db18a819
出典データセット
uspto-grants-1987_04
特許番号
US04657906

関連ノート

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