4-Fluorobenzonitrile → 2-[2-(4-Cyano-phenoxy)-1-hydroxy-1-methyl-ethyl]-6-trifluoromethyl-1H-indole-5-carbonitrile

HRID 32946

反応式

HRID 32946 の反応式
[OH:1][C:2]([C:6]1[NH:7][C:8]2[C:13]([CH:14]=1)=[CH:12][C:11]([C:15]#[N:16])=[C:10]([C:17]([F:20])([F:19])[F:18])[CH:9]=2)([CH3:5])[CH2:3][OH:4].[H-].[Na+].F[C:24]1[CH:31]=[CH:30][C:27]([C:28]#[N:29])=[CH:26][CH:25]=1>CN(C=O)C>[C:28]([C:27]1[CH:30]=[CH:31][C:24]([O:4][CH2:3][C:2]([C:6]2[NH:7][C:8]3[C:13]([CH:14]=2)=[CH:12][C:11]([C:15]#[N:16])=[C:10]([C:17]([F:20])([F:18])[F:19])[CH:9]=3)([OH:1])[CH3:5])=[CH:25][CH:26]=1)#[N:29]

参加物

5

反応物 3

HCID 145174-FluorobenzonitrileHCID 24758Sodium hydrideHCID 668644952-(1,2-Dihydroxy-1-methyl-ethyl)-6-trifluoromethyl-1H-indole-5-carbonitrile

生成物 1

HCID 668653412-[2-(4-Cyano-phenoxy)-1-hydroxy-1-methyl-ethyl]-6-trifluoromethyl-1H-indole-5-carbonitrile

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

To a solution of 2-(1,2-dihydroxy-1-methyl-ethyl)-6-trifluoromethyl-1-H-indole-5-carbonitrile (209.6 mg, 0.7374 mmol) in dry DMF (4 ml) was added NaH (60 mg, 1.4749 mmol, 60% in mineral oil). After the reaction mixture was stirred at room temperature for 30 min., 4-fluorobenzonitrile (98.15 mg, 0.8115 mmol) was added, and the reaction mixture stirred at room temperature. After HPLC indicated the consumption of starting material, the reaction mixture was poured onto water and extracted with ethyl acetate. The organic layer was washed with 10% LiCl, brine and dried over MgSO4. Column chromatography (EtOAc/Hexanes 50%-100%) yielded the title product as a light yellow powder.

後処理

  1. stirringthe reaction mixture stirred at room temperature
  2. customthe consumption of starting material
  3. additionthe reaction mixture was poured onto water
  4. extractionextracted with ethyl acetate
  5. washThe organic layer was washed with 10% LiCl, brine
  6. dry with materialdried over MgSO4

出典と根拠

ORDレコード
ord-f4b807ca9b7449daa594c1884e4c313f
出典データセット
uspto-grants-2008_09
特許番号
US07427682B2

関連ノート

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