Hydrazine → 3,5-Diphenyl-1H-pyridazin-4-one

HRID 597180Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 597180
C([N:3](CC)[CH:4]=[C:5]([C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)[C:6](=[O:15])[C:7]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)=O)C.[NH2:24]N>C(O)(C)C>[C:9]1([C:7]2[C:6](=[O:15])[C:5]([C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=3)=[CH:4][NH:3][N:24]=2)[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1

Komponenten

4

Versuchsvorschrift

The product solution from Example 1 was cooled to 0° C. and mixed with 20 ml. of isopropyl alcohol and 2 ml. of hydrazine. The mixture was stirred for 10 minutes, and was then warmed to room temperature and stirred for 15 hours. The product was then collected by filtration. The yield was 6.0 g. of 3,5-diphenyl-4(1H)-pyridazinone, m.p. 328°-32° C., which was identified by infrared and nuclear magnetic resonance analysis.

Aufarbeitung

  1. additionmixed with 20 ml
  2. stirringstirred for 15 hours
  3. filtrationThe product was then collected by filtration

Quellen und Nachweise

ORD-Eintrag
ord-a361d087769a4d7d99e2c6a35a6653cd
Quelldatensatz
uspto-grants-1977_03
Patentnummer
US04013658

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