ChemicalBook--->CAS DataBase List--->885275-59-2

885275-59-2

885275-59-2 Structure

885275-59-2 Structure
IdentificationBack Directory
[Name]

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

885275-59-2
[Synonyms]

6-CHLORO-3-IODO-IMIDAZO[1,2-A]PYRIDINE
Imidazo[1,2-a]pyridine, 6-chloro-3-iodo-
6-Chloro-3-iodoimidazo[1,2-a]pyridine,95%
[EINECS(EC#)]

604-604-1
[Molecular Formula]

C7H4ClIN2
[MDL Number]

MFCD06739217
[MOL File]

885275-59-2.mol
[Molecular Weight]

278.48
Chemical PropertiesBack Directory
[storage temp. ]

2-8°C, protect from light
[Appearance]

Off-white to light yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
Hazard InformationBack Directory
[Uses]

It is used as an intermediate in organic syntheses
[Synthesis]

6-CHLOROIMIDAZO[1,2-A]PYRIDINE

6188-25-6

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

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
Spectrum DetailBack Directory
[Spectrum Detail]

6-CHLORO-3-IODO-IMIDAZO[1,2-A]PYRIDINE(885275-59-2)1HNMR
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