Ethanol → HCID 21163089、化合物

HRID 1278221ノート

反応式

HRID 1278221 の反応式
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([C:7]2[N:12]3[N:13]=[CH:14][C:15]([C:16]([O:18][CH2:19][CH3:20])=O)=[C:11]3[N:10]=[CH:9][CH:8]=2)[CH:2]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-].C(O)C.O>CCOCC>[CH2:19]([O:18][CH2:16][C:15]1[CH:14]=[N:13][N:12]2[C:7]([C:3]3[CH:2]=[N:1][CH:6]=[CH:5][CH:4]=3)=[CH:8][CH:9]=[N:10][C:11]=12)[CH3:20]

参加物

6

実験手順

A mixture of 0.01 mole of ethyl 7-(3-pyridyl)pyrazolo[1,5-a]pyrimidine-3-carboxylate and lithium aluminum hydride in ether is heated at reflux temperature for 8 hours. To the mixture is added (dropwise) ethanol and water. The ethereal layer is separated, then ethanol and anhydrous hydrochloric acid is added to it. The resulting mixture is refluxed for 8 hours and the solvent is removed. The residue is extracted with dichloromethane. The dichloromethane extract is passed through a column of hydrous magnesium silicate. The eluent is concentrated and diluted with hexane to give the product of the example.

後処理

  1. temperatureis heated
  2. temperatureat reflux temperature for 8 hours
  3. customThe ethereal layer is separated
  4. additionethanol and anhydrous hydrochloric acid is added to it
  5. temperatureThe resulting mixture is refluxed for 8 hours
  6. customthe solvent is removed
  7. extractionThe residue is extracted with dichloromethane
  8. extractionThe dichloromethane extract
  9. concentrationThe eluent is concentrated
  10. additiondiluted with hexane
  11. customto give the product of the example

出典と根拠

ORDレコード
ord-950075dc42e64cff9c8cf51210904b93
出典データセット
uspto-grants-1981_07
特許番号
US04281000

反応ノート

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