Potassium Carbonate → HCID 66810481、化合物

HRID 455240ノート

反応式

HRID 455240 の反応式
[C:1]([C:3]1[CH:4]=[C:5]([N+:10]([O-:12])=[O:11])[CH:6]=[CH:7][C:8]=1F)#[N:2].[F:13][C:14]1[CH:19]=[CH:18][C:17]([OH:20])=[CH:16][C:15]=1[NH:21][C:22](=[O:34])[CH2:23][C:24]1[CH:29]=[CH:28][CH:27]=[C:26]([C:30]([F:33])([F:32])[F:31])[CH:25]=1.C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O.C(OCC)(=O)C>[C:1]([C:3]1[CH:4]=[C:5]([N+:10]([O-:12])=[O:11])[CH:6]=[CH:7][C:8]=1[O:20][C:17]1[CH:18]=[CH:19][C:14]([F:13])=[C:15]([NH:21][C:22](=[O:34])[CH2:23][C:24]2[CH:29]=[CH:28][CH:27]=[C:26]([C:30]([F:31])([F:32])[F:33])[CH:25]=2)[CH:16]=1)#[N:2]

参加物

6

実験手順

To a solution of 3-cyano-4-fluoronitrobenzene (0.530 g, 3.19 mmol) and N-(2-fluoro-5-hydroxyphenyl)-2-[3-(trifluoromethyl)phenyl]acetamide (1.00 g, 3.19 mmol) in N,N-dimethylformamide (5 mL) was added potassium carbonate (0.530 g, 3.83 mmol), and the mixture was stirred at room temperature for 4 hr. The reaction mixture was diluted with ethyl acetate (100 mL), washed successively with water (100 mL) and saturated brine (100 mL), and dried over anhydrous magnesium sulfate. Insoluble material was filtered off. The obtained organic layer was purified by basic silica gel column chromatography (eluate: 50% ethyl acetate/n-hexane), and the obtained solution was concentrated under reduced pressure to give the title compound (1.38 g, 94%) as a yellow oil.

後処理

  1. washwashed successively with water (100 mL) and saturated brine (100 mL)
  2. dry with materialdried over anhydrous magnesium sulfate
  3. filtrationInsoluble material was filtered off
  4. customThe obtained organic layer was purified by basic silica gel column chromatography (eluate: 50% ethyl acetate/n-hexane)
  5. concentrationthe obtained solution was concentrated under reduced pressure

出典と根拠

ORDレコード
ord-8835661e8c3046b3aaffe4b515171c59
出典データセット
uspto-grants-2013_07
特許番号
US08497274B2

反応ノート

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