Basic information Safety Supplier Related

6-CHLORO-3-IODO-IMIDAZO[1,2-A]PYRIDINE

Basic information Safety Supplier Related

6-CHLORO-3-IODO-IMIDAZO[1,2-A]PYRIDINE Basic information

Product Name:
6-CHLORO-3-IODO-IMIDAZO[1,2-A]PYRIDINE
Synonyms:
  • Imidazo[1,2-a]pyridine, 6-chloro-3-iodo-
  • 6-CHLORO-3-IODO-IMIDAZO[1,2-A]PYRIDINE
  • 6-Chloro-3-iodoimidazo[1,2-a]pyridine,95%
CAS:
885275-59-2
MF:
C7H4ClIN2
MW:
278.48
EINECS:
604-604-1
Mol File:
885275-59-2.mol
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6-CHLORO-3-IODO-IMIDAZO[1,2-A]PYRIDINE Chemical Properties

storage temp. 
2-8°C, protect from light
Appearance
Off-white to light yellow Solid
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6-CHLORO-3-IODO-IMIDAZO[1,2-A]PYRIDINE Usage And Synthesis

Uses

It is used as an intermediate in organic syntheses

Synthesis

6188-25-6

885275-59-2

General procedure for the synthesis of 6-chloro-3-iodoimidazo[1,2-a]pyridine from 6-chloroimidazo[1,2-A]pyridine: To a solution of 6-chloroimidazo[1,2-A]pyridine (500.00 mg, 3.28 mmol) in N,N-dimethylformamide (DMF, 10 mL) at 0 °C was added N-iodosuccinimide (NIS, 884.70 mg, 3.94 mmol). The reaction mixture was slowly warmed to 20 °C and stirred continuously for 16 hours. Upon completion of the reaction, the reaction was quenched by the addition of saturated sodium bicarbonate solution (20 mL) and stirring was continued for 1 hour. The resulting solid product was collected by filtration and dried in an oven to afford the target compound 6-chloro-3-iodoimidazo[1,2-a]pyridine (900.00 mg, 3.23 mmol). The product was characterized by 1H NMR (400 MHz, CDCl3) with chemical shifts of δH 8.20 (s, 1H), 7.72 (s, 1H), 7.57 (d, 1H), 7.21 (dd, 1H).

References

[1] Patent: WO2018/98500, 2018, A1. Location in patent: Page/Page column 80; 81

6-CHLORO-3-IODO-IMIDAZO[1,2-A]PYRIDINESupplier

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