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3-Chloro-6-morpholinopyridazine

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3-Chloro-6-morpholinopyridazine Basic information

Product Name:
3-Chloro-6-morpholinopyridazine
Synonyms:
  • 4-(6-CHLORO-3-PYRIDAZINYL)MORPHOLINE
  • 4-(6-CHLOROPYRIDAZIN-3-YL)MORPHOLINE
  • 3-CHLORO-6-MORPHOLINOPYRIDAZINE
  • JR-8760, 4-(6-Chloropyridazin-3-yl)morpholine, 97%
  • 1-(6-Chloropyridazino-3-yl)morpholine
  • 3-Chloro-6-morpholinopyridazine ,97%
  • 3-chloro-6-morpholin-4-ylpyridazine
  • 3-chloro-6-morpholin-4-yl-pyridazine
CAS:
17259-32-4
MF:
C8H10ClN3O
MW:
199.64
Product Categories:
  • alkyl chloride
  • Amines
  • blocks
Mol File:
17259-32-4.mol
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3-Chloro-6-morpholinopyridazine Chemical Properties

storage temp. 
-20°C, sealed storage, away from moisture and light
form 
solid
Appearance
White to light yellow Solid
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
22-36/37/38
Safety Statements 
26-36
HazardClass 
IRRITANT
HS Code 
29335990
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3-Chloro-6-morpholinopyridazine Usage And Synthesis

Chemical Properties

Off-white powder

Synthesis

110-91-8

141-30-0

17259-32-4

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 morpholine (5.03 mmol). The reaction mixture was refluxed in ethanol (for 3,6-dichloropyridazine and 2,6-dichloropyrazine) or stirred at room temperature (for 2,4-dichloropyrimidine). The reaction process is monitored by gas chromatography (GC). After 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 the pure 4-(6-chloropyridazin-3-yl)morpholine.

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] Patent: WO2005/92899, 2005, A1. Location in patent: Page/Page column 87
[5] Bioorganic and Medicinal Chemistry, 2007, vol. 15, # 4, p. 1586 - 1605

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