Basic information Safety Supplier Related

3,6-Dichloro[1,2,4]triazolo[4,3-b]pyridazine

Basic information Safety Supplier Related

3,6-Dichloro[1,2,4]triazolo[4,3-b]pyridazine Basic information

Product Name:
3,6-Dichloro[1,2,4]triazolo[4,3-b]pyridazine
Synonyms:
  • 3,6-Dichloro-s-triazolo[4,3-b]pyridazine
  • 1,2,4-Triazolo[4,3-b]pyridazine, 3,6-dichloro-
CAS:
33050-38-3
MF:
C5H2Cl2N4
MW:
189
Product Categories:
  • Halides
  • Fused Ring Systems
  • Building Blocks
  • Imidazo[x,x-y]pyridazine
Mol File:
33050-38-3.mol
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3,6-Dichloro[1,2,4]triazolo[4,3-b]pyridazine Chemical Properties

Melting point:
140-143°C
Density 
1.90
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
solid
pka
-2.88±0.30(Predicted)
color 
Yellow-brown
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Safety Information

Hazard Codes 
Xi
HazardClass 
IRRITANT
HS Code 
2933998090
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3,6-Dichloro[1,2,4]triazolo[4,3-b]pyridazine Usage And Synthesis

Synthesis

33050-32-7

33050-38-3

The general procedure for the synthesis of 3,6-dichloro-[1,2,4]triazolo[4,3-b]pyridazine using 6-chloro-[1,2,4]triazolo[4,3-b]pyridazin-3(2H)-one as starting material is as follows: 6-chloro-[1,2,4]triazolo[4,3-b]pyridazin-3(2H)-one (1 eq.) was added to phosphorochloridic acid (10 eq.). The reaction mixture was heated to reflux and maintained for 20 hours. After completion of the reaction, the mixture was evaporated to dryness. The residue was dissolved in ethyl acetate and washed with saturated aqueous potassium carbonate. The organic layer was dried over anhydrous sodium sulfate, filtered and evaporated to dryness to give Intermediate D in 93% yield. The product was a pale yellow solid.1H NMR (MeOD-d4) data were as follows: δ 7.51 (dd, 1H, J = 9.6Hz, 0.9Hz); δ 8.30 (dd, 1H, J = 9.6Hz, 0.9Hz).

References

[1] Patent: WO2013/45519, 2013, A1. Location in patent: Page/Page column 43

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