Hydrazine → HCID 178509108, Verbindung

HRID 2230383Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2230383
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=O)[CH:9]([C:12]2[CH:17]=[CH:16][N:15]=[CH:14][CH:13]=2)[C:10]#[N:11])=[CH:4][CH:3]=1.P(Cl)(Cl)Cl.[NH2:23][NH2:24]>C(#N)C>[NH2:11][C:10]1[NH:24][N:23]=[C:8]([C:5]2[CH:6]=[CH:7][C:2]([Cl:1])=[CH:3][CH:4]=2)[C:9]=1[C:12]1[CH:17]=[CH:16][N:15]=[CH:14][CH:13]=1

Komponenten

5

Versuchsvorschrift

A solution of 3-(4-chlorophenyl)-3-oxo-2-(pyridin-4-yl)propanenitrile (3.50 g, 13.6 mmol) in 40 mL acetonitrile and phosphorous trichloride (14.2 ml, 163 mmol) was stirred at 100° C. for 5 hours. The reaction mixture was concentrated in vacuo, and the residue taken up in toluene and concentrated again. The residue was then taken up in ethanol (150 mL) and treated with anhydrous hydrazine (1.71 mL, 54.4 mmol). The reaction mixture was heated to reflux for 3 hours, cooled, and concentrated in vacuo. The residue was triturated with a mixture of ethanol and dichloromethane (1:4), and filtered. The solid was washed with the ethanol/dichloromethane mixture, and dried to give 5-amino-3-(4-chlorophenyl)-4-(pyridin-4-yl)-pyrazole (2.0 g, 54%): m.p. >300° C. 1H NMR (DMSO/300 MHz) δ8.40 (d, 2H), 7.40 (d, 2H), 7.29 (d, 2H), 7.11 (d, 2H), 5.05 (s, 2H). ESLRMS m/z 271 (M+H). ESHRMS m/z 271.0752 (M+H, C14H11N4Cl requires 271.0750).

Aufarbeitung

  1. concentrationThe reaction mixture was concentrated in vacuo
  2. concentrationconcentrated again
  3. temperatureThe reaction mixture was heated
  4. temperatureto reflux for 3 hours
  5. temperaturecooled
  6. concentrationconcentrated in vacuo
  7. customThe residue was triturated with a mixture of ethanol and dichloromethane (1:4)
  8. filtrationfiltered
  9. washThe solid was washed with the ethanol/dichloromethane mixture
  10. customdried

Quellen und Nachweise

ORD-Eintrag
ord-9bc16b4934de438b8f13719faf78cdc3
Quelldatensatz
uspto-grants-2002_07
Patentnummer
US06423713B1

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