8-Bromo-6-chloroimidazo[1,2-a]pyridine
8-Bromo-6-chloroimidazo[1,2-a]pyridine Basic information
- Product Name:
- 8-Bromo-6-chloroimidazo[1,2-a]pyridine
- Synonyms:
-
- 8-Bromo-6-chloroimidazo[1,2-a]pyridine
- IMidazo[1,2-a]pyridine, 8-broMo-6-chloro-
- 6-chloro-8-bromoimidazo[1,2-a]pyridine
- CAS:
- 957187-27-8
- MF:
- C7H4BrClN2
- MW:
- 231.48
- Mol File:
- 957187-27-8.mol
8-Bromo-6-chloroimidazo[1,2-a]pyridine Chemical Properties
- Melting point:
- 125-128℃
- Density
- 1.84±0.1 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- pka
- 2.23±0.50(Predicted)
- Appearance
- White to off-white Solid
- Water Solubility
- Slightly soluble in water.
8-Bromo-6-chloroimidazo[1,2-a]pyridine Usage And Synthesis
Uses
8-Bromo-6-chloroimidazo[1,2-a]pyridine is used as an organic chemical synthesis intermediate.
Synthesis
107-20-0
26163-03-1
957187-27-8
3-Bromo-5-chloropyridin-2-amine (10 g, 49 mmol) and chloroacetaldehyde (50% aqueous, 12 mL, 98 mmol) were mixed in ethanol (100 mL) and the reaction was heated at 50 °C overnight. Upon completion of the reaction, the mixture was cooled to room temperature and concentrated. To the concentrated residue was added acetone (30 mL) and stirred rapidly for 2 hours. The resulting solid was collected by filtration and dried to afford the target product 8-bromo-6-chloroimidazo[1,2-a]pyridine (10.0 g, 89% yield). Mass spectrometry analysis showed [M + H]+ peak of 231. 1H NMR (500 MHz, DMSO) data were as follows: δ 9.20 (s, 1H), 8.33 (s, 1H), 8.29 (s, 1H), 8.09 (s, 1H).
References
[1] Patent: US2013/116262, 2013, A1. Location in patent: Paragraph 0195; 0196; 0197
[2] Patent: WO2011/72064, 2011, A1. Location in patent: Page/Page column 74
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8-Bromo-6-chloroimidazo[1,2-a]pyridine(957187-27-8)Related Product Information
- 8-Bromo-6-methylimidazo[1,2-a]pyridine
- Ethyl 8-bromo-6-chloroimidazo[1,2-a]pyridine-2-carboxylate
- 8-Bromo-6-chloroimidazo[1,2-a]pyrazine
- 6-BROMO-8-METHYLIMIDAZO[1,2-A]PYRIDINE
- Imidazo[1,2-a]pyridine
- NSC 304613
- IMidazo[1,2-a]pyridine-8-carboxylic acid, 3-broMo-, ethyl ester
- IMidazo[1,2-a]pyridine, 6,8-dibroMo-
- Ethyl Imidazo[1,2-a]pyridine-3-carboxylate
- IMidazo[1,2-a]pyridine-3-carboxylic acid, 6-chloro-, ethyl ester
- IMidazo[1,2-a]pyridine-3-carboxylic acid, 6-broMo-, ethyl ester
- IMidazo[1,2-a]pyridine, 6-broMo-5-chloro-
- 8-BroMo-4,4-diMethyl-3,4-dihydroquinolin-2(1H)-one
- 8-bromo-5-fluoroquinoline
- Quinoline, 8-bromo-5-methyl- (9CI)
- 8-BROMO-4-CHLOROQUINOLINE
- 6-Chloro-5-methyl-imidazo[1,2-a]pyridine
- IMidazo[1,2-a]pyridine, 5-chloro-7-Methyl-