N,N-Diethylaniline → 7-Chloro-5-methyl-3-(2,4,6-trimethyl-phenyl)-pyrazolo[1,5-a]pyrimidine

Reaktionsgleichung

[CH3:1][C:2]1[NH:3][C:4]2[N:5]([N:9]=[CH:10][C:11]=2[C:12]2[C:17]([CH3:18])=[CH:16][C:15]([CH3:19])=[CH:14][C:13]=2[CH3:20])[C:6](=O)[CH:7]=1.CCN(C1C=CC=CC=1)CC.O=P(Cl)(Cl)[Cl:34]>>[Cl:34][C:6]1[N:5]2[N:9]=[CH:10][C:11]([C:12]3[C:17]([CH3:18])=[CH:16][C:15]([CH3:19])=[CH:14][C:13]=3[CH3:20])=[C:4]2[N:3]=[C:2]([CH3:1])[CH:7]=1

Komponenten

Edukt 3

HCID 7061N,N-Diethylaniline

HCID 24813Phosphorus oxychloride

HCID 178424609HCID 178424609, Verbindung

Produkt 1

HCID 224743217-Chloro-5-methyl-3-(2,4,6-trimethyl-phenyl)-pyrazolo[1,5-a]pyrimidineAusbeute 94 %

Versuchsvorschrift

A suspension of 5-methyl-3-(2,4,6-trimethyl-phenyl)-4H-pyrazolo[1,5-a]pyrimidin-7-one (590 mg, 2.2 mmol) in 9 ml of POCl3 was treated with diethylaniline (0.7 ml) and the resulting mixture was stirred at reflux for 15 hours. The reaction mixture was concentrated to dryness. The residue was treated with ice water and stirred for 20 min, then extracted with chloroform. The organic layer was dried and concentrated to yield an orange oil which crystallized upon standing. The material was purified through silica gel column chromatography using chloroform as eluent to give 590 mg (94%) of the title compound as a yellow solid; 1H NMR (CDCl3) ä 8.08(s, 1H), 6.98(s, 2H), 6.86(s, 1H), 2.56(s, 3H), 2.33(s, 3H), 2.09(s, 6H) ppm.