Basic information Safety Supplier Related

6-chloro-2-Methyl-3-broMo-iMidazo[1,2-b]pyridazine

Basic information Safety Supplier Related

6-chloro-2-Methyl-3-broMo-iMidazo[1,2-b]pyridazine Basic information

Product Name:
6-chloro-2-Methyl-3-broMo-iMidazo[1,2-b]pyridazine
Synonyms:
  • 6-chloro-2-Methyl-3-broMo-iMidazo[1,2-b]pyridazine
  • IMidazo[1,2-b]pyridazine, 3-broMo-6-chloro-2-Methyl-
  • 3-broMo-6-chloro-2-Methly-iMidazo [1, 2-b] pyridazine
  • 6-chloro-2-Methyl-3-broMo-iMidazopyridazine
CAS:
18112-31-7
MF:
C7H5BrClN3
MW:
246.49
Mol File:
18112-31-7.mol
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6-chloro-2-Methyl-3-broMo-iMidazo[1,2-b]pyridazine Chemical Properties

Melting point:
154 °C
Density 
1.90±0.1 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
1.75±0.30(Predicted)
Appearance
White to yellow Solid
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6-chloro-2-Methyl-3-broMo-iMidazo[1,2-b]pyridazine Usage And Synthesis

Synthesis

14793-00-1

18112-31-7

The general procedure for the synthesis of 6-chloro-2-methyl-3-bromo-imidazo[1,2-b]pyrazines using 6-chloro-2-methylimidazo[1,2-b]pyridazine as starting material was as follows: 6-chloro-2-methylimidazo[1,2-b]pyridazine (2.00 g, 11.9 mmol, 1.0 eq.) was dissolved in chloroform (50 mL), followed by N-bromosuccinimide (2.55 g, 14.3 mmol, 1.2 eq.). The reaction mixture was stirred at room temperature for 15 hours. Upon completion of the reaction, the product was purified by column chromatography using a hexane solution of 50% ethyl acetate as eluent, resulting in 2.64 g of yellow solid product in 90% yield.

References

[1] Patent: US2014/256733, 2014, A1. Location in patent: Paragraph 0266; 0269-0270
[2] Patent: WO2008/52733, 2008, A1. Location in patent: Page/Page column 81

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