6-Chloro-3-iodo-imidazo[1,2-a]pyridine

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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-iodoimidazo[1,2-a]pyridine,95%;6-Chloro-3-iodo-imidazo[1,2-a]pyridine
CAS:885275-59-2
MF:C7H4ClIN2
MW:278.48
EINECS:604-604-1
Product Categories:
Mol File:885275-59-2.mol
6-Chloro-3-iodo-imidazo[1,2-a]pyridine Structure
6-Chloro-3-iodo-imidazo[1,2-a]pyridine Chemical Properties
storage temp. 2-8°C, protect from light
AppearanceOff-white to light yellow Solid
Safety Information
MSDS Information
6-Chloro-3-iodo-imidazo[1,2-a]pyridine Usage And Synthesis
UsesIt 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
6-Chloro-3-iodo-imidazo[1,2-a]pyridine Preparation Products And Raw materials
Raw materials6-Chloroimidazo[1,2-a]pyridine-->N,N-Dimethylformamide-->N-Iodosuccinimide
Tag:6-Chloro-3-iodo-imidazo[1,2-a]pyridine(885275-59-2) Related Product Information
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