Water → methyl 6-(1H-pyrazol-1-yl)nicotinate

HRID 1009919

反応式

HRID 1009919 の反応式
[NH:1]1[CH:5]=[CH:4][CH:3]=C1.[H-].[Na+].Cl[C:9]1[CH:18]=[CH:17][C:12]([C:13]([O:15][CH3:16])=[O:14])=[CH:11][N:10]=1.O.C[N:21](C=O)C>>[N:1]1([C:9]2[CH:18]=[CH:17][C:12]([C:13]([O:15][CH3:16])=[O:14])=[CH:11][N:10]=2)[CH:5]=[CH:4][CH:3]=[N:21]1

参加物

6

反応物 5

HCID 962WaterHCID 6228DimethylformamideHCID 8027PyrroleHCID 24758Sodium hydrideHCID 254249Methyl 6-chloropyridine-3-carboxylate

生成物 1

HCID 3741563methyl 6-(1H-pyrazol-1-yl)nicotinate収率 64%

実験手順

To a suspension of pyrrole (0.356 g, 5.23 mmol) in DMF (20 ml) was added sodium hydride (60% in oil, 0.233 g, 5.81 mmol). After stirring for 5 hrs., methyl 6-chloronicotinate (1.00 g, 5.81 mmol) was added, and the mixture was further stirred for 27 hrs. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine and dried (over anhydrous MgSO4). After concentration under reduced pressure, the precipitated solid was collected by filtration and washed with hexane to give the title compound (0.683 g, 64%) as a colorless powder.

後処理

  1. stirringthe mixture was further stirred for 27 hrs
  2. extractionthe mixture was extracted with ethyl acetate
  3. washThe extract was washed with saturated brine
  4. dry with materialdried (over anhydrous MgSO4)
  5. concentrationAfter concentration under reduced pressure
  6. filtrationthe precipitated solid was collected by filtration
  7. washwashed with hexane

出典と根拠

ORDレコード
ord-aa8c175cd710439180fe9316dc9635d3
出典データセット
uspto-grants-2011_07
特許番号
US07973163B2

関連ノート

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