Sodium Carbonate → 4-Bromo-1H-indole-2-carbonitrile

HRID 2365161ノート

反応式

HRID 2365161 の反応式
P(Cl)(Cl)(Cl)=O.[Br:6][C:7]1[CH:15]=[CH:14][CH:13]=[C:12]2[C:8]=1[CH:9]=[C:10]([C:16]([NH2:18])=O)[NH:11]2.C([O-])([O-])=O.[Na+].[Na+]>C1(C)C=CC=CC=1>[Br:6][C:7]1[CH:15]=[CH:14][CH:13]=[C:12]2[C:8]=1[CH:9]=[C:10]([C:16]#[N:18])[NH:11]2

参加物

5

反応物 3

HCID 10340Sodium CarbonateHCID 24813Phosphorus oxychlorideHCID 591512734-bromo-1H-indole-2-carboxamide

生成物 1

HCID 591513014-Bromo-1H-indole-2-carbonitrile収率 82.3%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

Phosphorous oxychloride (1.9 mL, 20 mmol) was added to a suspension of 4-bromo-1H-indole-2-carboxylic acid amide (1.32 g, 5.5 mmol.) in toluene (10 mL) and the mixture was stirred at reflux for 45 min. On cooling, the mixture was poured into an aqueous Na2CO3 solution (sat., 50 mL) and the mixture stirred until effervescence had subsided. The layers were separated, the aqueous phase extracted with EtOAc and the combined organic layers dried (MgSO4) and evaporated to dryness. The crude material was purified by column chromatography to afford the title compound as a solid (1.00 g, 82%).

後処理

  1. temperatureat reflux for 45 min
  2. temperatureOn cooling
  3. stirringthe mixture stirred until effervescence
  4. customThe layers were separated
  5. extractionthe aqueous phase extracted with EtOAc
  6. dry with materialthe combined organic layers dried (MgSO4)
  7. customevaporated to dryness
  8. customThe crude material was purified by column chromatography

出典と根拠

ORDレコード
ord-6ddc06bd0bf048cbac98276d23aa3f70
出典データセット
uspto-grants-2014_04
特許番号
US08697693B2

反応ノート

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