1-(3-Pyridyl)-3-(dimethylamino)-2-propen-1-one → 7-(3-Pyridinyl)[1,2,4]triazolo[1,5-a]pyrimidine

HRID 326089

反応式

HRID 326089 の反応式
[NH2:1][C:2]1[N:6]=[CH:5][NH:4][N:3]=1.CN(C)[CH:9]=[CH:10][C:11]([C:13]1[CH:14]=[N:15][CH:16]=[CH:17][CH:18]=1)=O>C(O)(=O)C>[N:15]1[CH:16]=[CH:17][CH:18]=[C:13]([C:11]2[N:3]3[N:4]=[CH:5][N:6]=[C:2]3[N:1]=[CH:9][CH:10]=2)[CH:14]=1

参加物

4

反応物 2

HCID 5670331-(3-Pyridyl)-3-(dimethylamino)-2-propen-1-oneHCID 178418311HCID 178418311、化合物

生成物 1

HCID 9009447-(3-Pyridinyl)[1,2,4]triazolo[1,5-a]pyrimidine

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

実験手順

A mixture of 2.54 g of 3-amino-1,2,4-triazole, 5.29 g of 3-dimethylamino-1-(3-pyridyl)-2-propene-1-one and 25 ml of glacial acetic acid was heated under reflux for 6 hours. The solvent was removed in vacuo and the solid residue was partitioned between a saturated aqueous sodium bicarbonate solution and dichloromethane. The organic layer was separated and dried over powdered anhydrous sodium sulfate. This solution was passed through a short column of a hydrous magnesium silicate and the effluent was refluxed on a steam bath with the gradual addition of hexane until crystallization was noted. On cooling the desired compound was separated and collection by filtration gave 1.95 g. of colorless crystals mp. 209°-210° C.

後処理

  1. temperaturewas heated
  2. temperatureunder reflux for 6 hours
  3. customThe solvent was removed in vacuo
  4. customthe solid residue was partitioned between a saturated aqueous sodium bicarbonate solution and dichloromethane
  5. customThe organic layer was separated
  6. customdried
  7. temperaturethe effluent was refluxed on a steam bath with the gradual addition of hexane until crystallization
  8. temperatureOn cooling the desired compound
  9. customwas separated
  10. customcollection
  11. filtrationby filtration
  12. customgave 1.95 g

出典と根拠

ORDレコード
ord-71b0cc88388149b8b5c31ae457814789
出典データセット
uspto-grants-1984_04
特許番号
US04444774

関連ノート

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