Réaction #2254150

Équation de réaction

acetic anhydride

ethyl acetate

triethylamine

acetic anhydride

1H-pyrazol-4-amine

dichloromethane

triethylamine

→

N-(1-acetyl-1H-pyrazol-4-yl)acetamide

Conditions de réaction

Traitement

1. 1
   Températurethe reaction was heated at 30° C. for an additional 3 hours
2. 2
   Autreto give a dark solution
3. 3
   AutreThe reaction mixture was purified by flash column chromatography
4. 4
   workup.ADDITIONThe fractions containing pure product
5. 5
   Concentrationconcentrated to dryness
6. 6
   Autreto afford an off-white solid
7. 7
   AutreThe solid was dried under vacuum at room temperature for 18 hours (5.55 g, 55%)

Mode opératoire

A 250-mL 3-neck flask was charged with 1H-pyrazol-4-amine (5 g, 60.2 mmol) and dichloromethane (50 mL). The resulting suspension was cooled to 5° C. and triethylamine (TEA, 9.13 g, 90.0 mmol) was added, followed by acetic anhydride (Ac2O, 7.37 g, 72.2 mmol) at <20° C. The reaction was stirred at room temperature for 18 h, at which point thin layer chromatography [Eluent: ethyl acetate] analysis indicated that the reaction was incomplete. Additional triethylamine (4.57 g, 45.0 mmol) and acetic anhydride (3.70 g, 36.0 mmol) were added and the reaction was heated at 30° C. for an additional 3 hours to give a dark solution, at which point thin layer chromatography analysis indicated that only a trace of starting material remained. The reaction mixture was purified by flash column chromatography using ethyl acetate as eluent. The fractions containing pure product were combined and concentrated to dryness to afford an off-white solid. The solid was dried under vacuum at room temperature for 18 hours (5.55 g, 55%): 1H NMR (400 MHz, DMSO-d6) δ 10.30 (s, 1H), 8.39 (d, J=0.7 Hz, 1H), 7.83 (d, J=0.7 Hz, 1H), 2.60 (s, 3H), 2.03 (s, 3H); EIMS m/z 167 ([M]+).

Source