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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 370444Erstellt: 24. Oktober 2026

Piperidine → 7-Methyl-6-piperidino-s-triazolo[4,3-b]pyridazine

https://huagongshe.com/de/reaction/370444

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPiperidineHCID 8082—
Edukt6-Chloro-7-methyl-[1,2,4]triazolo[4,3-b]pyridazineHCID 819796—
LösungsmittelEthanolHCID 702—
Produkt7-Methyl-6-piperidino-s-triazolo[4,3-b]pyridazineHCID 13518811—

Reaktionsschritte

7.8 Grams (0.0462 mole) of the 6-chloro-7-methyl-s-triazolo[4,3-b]pyridazine is mixed with 7.86 grams (0.0924 mole) of piperidine in 50 ml of ethanol. The mixture is heated at reflux temperature for 4 hours. The mixture is concentrated by evaporation and the residue of the reaction mixture is partitioned between aqueous sodium bicarbonate solution and methylene chloride. The methylene chloride layer is separated, dried over anhydrous sodium sulfate and evaporated to dryness under reduced pressure. The 7-methyl-6-piperidino-s-triazolo[4,3-b]pyridazine product is obtained as a residue from the evaporation. The product is recrystallized from hexane and found to melt at 78°-79° C. The structure of the product is confirmed by infrared spectroscopy, by nuclear magnetic resonance analysis, and by elemental analysis. (Calculated for C11H15N5 : C, 60.80; H, 6.96; N, 32.24. Found: C, 60.40; H, 6.98; N, 32.17.)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04526890
Quelldatensatzuspto-grants-1985_07
ORD IDord-c64ff2a37c474fefa41ee9101a711494
Quellennotizuspto-grants-1985_07