Acetic Acid → 3-Methyl-1-(pyridin-2-yl)-1H-pyrazol-5-amine

HRID 497933

Reaktionsgleichung

Reaktionsgleichung von HRID 497933
N/[C:2](=[CH:5]\[CH3:6])/[C:3]#[N:4].[NH:7]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][N:10]=1)[NH2:8].C(O)(=O)C>C(O)C>[CH3:6][C:5]1[CH:2]=[C:3]([NH2:4])[N:7]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][N:10]=2)[N:8]=1

Komponenten

5

Versuchsvorschrift

To an ice-cold solution of aminocrotononitrile (82 g, 1.0 mol) and 2-hydrazinopyridine (120 g, 1.1 mol) in ethanol (300 mL) was added acetic acid (132 g, 2.2 mol), and the mixture was heated under reflux for 3.5 hours. After the mixture was allowed to cool to room temperature, the reaction solvent was evaporated under reduced pressure and water was added to the residue. After the solution was made basic by the addition of an aqueous sodium hydroxide solution, organic matter was extracted with ethyl acetate. The extract was washed with saturated brine and water and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. Purification of the residue by silica gel column chromatography (ethyl acetate) gave the title compound (156.3 g, 90% yield).

Aufarbeitung

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for 3.5 hours
  3. customthe reaction solvent was evaporated under reduced pressure and water
  4. additionwas added to the residue
  5. additionAfter the solution was made basic by the addition of an aqueous sodium hydroxide solution, organic matter
  6. extractionwas extracted with ethyl acetate
  7. washThe extract was washed with saturated brine and water
  8. dry with materialdried over anhydrous magnesium sulfate
  9. customthe solvent was evaporated under reduced pressure
  10. customPurification of the residue by silica gel column chromatography (ethyl acetate)

Quellen und Nachweise

ORD-Eintrag
ord-608a2beee47140a2a93a373efc43f977
Quelldatensatz
uspto-grants-2005_09
Patentnummer
US06949648B2

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