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1-(6-Chloro-pyridazino-3-yl)piperidine

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1-(6-Chloro-pyridazino-3-yl)piperidine Basic information

Product Name:
1-(6-Chloro-pyridazino-3-yl)piperidine
Synonyms:
  • 3-CHLORO-6-PIPERIDIN-1-YL-PYRIDAZINE
  • 3-CHLORO-6-(1-PIPERIDINYL)PYRIDAZINE
  • 1-(6-CHLORO-PYRIDAZINO-3-YL)PIPERIDINE
  • 3-Chloro-6-piperidinopyridazine
  • 3-CHLORO-6-(1-PIPERIDINYL)PYRIDAZINE
  • 3-chloro-6-(1-piperidyl)pyridazine
  • Pyridazine, 3-chloro-6-(1-piperidinyl)-
  • 1-(6-Chloro-pyridazino-3-yl)piperidine ISO 9001:2015 REACH
CAS:
1722-11-8
MF:
C9H12ClN3
MW:
197.66
EINECS:
200-001-2
Mol File:
1722-11-8.mol
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1-(6-Chloro-pyridazino-3-yl)piperidine Chemical Properties

Melting point:
80~82℃
Boiling point:
388.6±27.0 °C(Predicted)
Density 
1.234±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
3.62±0.10(Predicted)
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Safety Information

Hazard Codes 
Xi
HazardClass 
IRRITANT
HS Code 
2933998090
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1-(6-Chloro-pyridazino-3-yl)piperidine Usage And Synthesis

Synthesis

110-89-4

141-30-0

1722-11-8

GENERAL METHOD: Anhydrous ethanol (5 mL) and 3,6-dichloropyridazine (3.36 mmol) were added to a 50 mL round-bottomed flask, followed by triethylamine (5.03 mmol) and hexahydropyridine (5.03 mmol). The reaction mixture was stirred under ethanol reflux conditions for 3,6-dichloropyridazine and 3,6-dichloropyrazine and at room temperature for 3,6-dichloropyrimidine. The reaction process was monitored by gas chromatography (GC). When the starting material 3,6-dichloropyridazine was completely consumed, the reaction mixture was poured into saturated ammonium chloride solution (20 mL) and extracted with dichloromethane (3 x 20 mL). The organic layers were combined, dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The crude product was ground with petroleum ether and filtered through a Büchner funnel to give pure 1-(6-chloropyridazin-3-yl)piperidine.

References

[1] Tetrahedron, 2015, vol. 71, # 29, p. 4859 - 4867
[2] Journal of Organic Chemistry, 2013, vol. 78, # 2, p. 370 - 379
[3] European Journal of Medicinal Chemistry, 2015, vol. 95, p. 277 - 301
[4] Yakugaku Zasshi, 1954, vol. 74, p. 1195,1197
[5] Chem.Abstr., 1955, p. 14768

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