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Water → 1-ethyl-2-(4-methylphenyl)-5-nitro-1H-pyrrolo[2,3-b]pyridine

HRID 541064
ノート
印刷プレビュー

反応式

HRID 541064 の反応式
[CH3:1][C:2](C)([O-])C.[K+].[N+:7]([C:10]1[CH:11]=[C:12]([C:17]#[C:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[C:13]([NH2:16])=[N:14][CH:15]=1)([O-:9])=[O:8].I[CH2:26]C.O>CN(C=O)C.CCOC(C)=O>[CH2:1]([N:16]1[C:13]2=[N:14][CH:15]=[C:10]([N+:7]([O-:9])=[O:8])[CH:11]=[C:12]2[CH:17]=[C:18]1[C:19]1[CH:24]=[CH:23][C:22]([CH3:26])=[CH:21][CH:20]=1)[CH3:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 962WaterHCID 6340IodoethaneHCID 23665647Potassium tert-butoxideHCID 593229015-Nitro-3-(phenylethynyl)pyridin-2-amine

生成物 1

HCID 672852781-ethyl-2-(4-methylphenyl)-5-nitro-1H-pyrrolo[2,3-b]pyridine

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide溶媒2 回
HCID 8857Ethyl Acetate溶媒

実験手順

To a suspension of potassium ter-butoxide (0.41 g, 3.7 mmol) in anhydrous DMF (5 ml) a solution of 5-nitro-3-(phenylethynyl)pyridin-2-amine (0.70 g, 2.8 mmol), in DMF (25 ml) was added dropwise while stirring at room temperature. After 1.5 days, iodoethane (0.38 ml, 4.7 mmol) was added and the whole stirred for additional 1.5 days. To the reaction H2O (50 ml) and EtOAc (100 ml) were then added. The mixture was poured into a separatory funnel, the organic layer separated, the aqueous one thoroughly extracted with EtOAc (50 ml) and combined organic layers washed with brine (2×100 ml). The organic solvent was removed by evaporation under reduced pressure and the residue was purified by column chromatography on silica gel (Et2O/n-hexane, Et2O 10%→20%) to give 1-ethyl-2-(4-methylphenyl)-5-nitro-1H-pyrrolo[2,3-b]pyridine:

後処理

  1. stirringthe whole stirred for additional 1.5 days
  2. additionwere then added
  3. additionThe mixture was poured into a separatory funnel
  4. customthe organic layer separated
  5. extractionthe aqueous one thoroughly extracted with EtOAc (50 ml)
  6. washwashed with brine (2×100 ml)
  7. customThe organic solvent was removed by evaporation under reduced pressure
  8. customthe residue was purified by column chromatography on silica gel (Et2O/n-hexane, Et2O 10%→20%)

出典と根拠

ORDレコード
ord-5ad3d8841c9647509a1651858f706d34
出典データセット
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08871948B2

反応ノート

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