Hydrochloric Acid → HCID 68677988、化合物

HRID 1993924ノート

反応式

HRID 1993924 の反応式
CO[C:3](=[O:16])[CH2:4][C:5](=O)[CH2:6][CH2:7][C:8]1[CH:13]=[CH:12][C:11]([F:14])=[CH:10][CH:9]=1.[F:17][C:18]1[CH:23]=[CH:22][C:21]([NH:24][NH2:25])=[CH:20][CH:19]=1.Cl.CCOC(C)=O>C(O)(=O)C.O>[F:17][C:18]1[CH:23]=[CH:22][C:21]([N:24]2[C:3](=[O:16])[CH2:4][C:5]([CH2:6][CH2:7][C:8]3[CH:9]=[CH:10][C:11]([F:14])=[CH:12][CH:13]=3)=[N:25]2)=[CH:20][CH:19]=1

参加物

7

反応物 4

HCID 313Hydrochloric AcidHCID 8857Ethyl AcetateHCID 69982(4-Fluorophenyl)hydrazineHCID 66789979500367-64-6

生成物 1

HCID 68677988HCID 68677988、化合物

試薬・触媒・溶媒 2

HCID 176Acetic Acid溶媒HCID 962Water溶媒

実験手順

To a solution of 5-(4-fluoro-phenyl)-3-oxo-pentanoic acid methyl ester (0.43 g) in acetic acid (5 mL) in a sealable tube was added 4-fluorophenylhydrazine.HCl (0.31 g). The reaction vessel was sealed and immersed into an oil bath at 100° C. for 18 hours. The reaction vessel was cooled to ambient temperature, opened and the contents were poured onto a mixture of EtOAc and water. The aqueous phase was extracted with EtOAc and the combined organic phases were washed with water and dried over sodium sulfate. Filtration and evaporation of the volatiles in vacuo afforded a crude crystalline material. The crude product was washed with ether to afford the desired 2-(4-fluoro-phenyl)-5-[2-(4-fluoro-phenyl)-ethyl]-2,4-dihydro-pyrazol-3-one (0.37 g) as a beige crystalline solid. MS (ESI+): 301.1 [M+H]+).

後処理

  1. customThe reaction vessel was sealed
  2. extractionThe aqueous phase was extracted with EtOAc
  3. washthe combined organic phases were washed with water
  4. dry with materialdried over sodium sulfate
  5. filtrationFiltration and evaporation of the volatiles in vacuo
  6. customafforded a crude crystalline material
  7. washThe crude product was washed with ether

出典と根拠

ORDレコード
ord-00157bec1a6a4e4b8037323192c2c75b
出典データセット
uspto-grants-2010_01
特許番号
US07652057B2

反応ノート

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