IMIDAZO[1,2-A]PYRIDINE-8-CARBOXYLIC ACID
IMIDAZO[1,2-A]PYRIDINE-8-CARBOXYLIC ACID Basic information
- Product Name:
- IMIDAZO[1,2-A]PYRIDINE-8-CARBOXYLIC ACID
- Synonyms:
-
- IMIDAZO[1,2-A]PYRIDINE-8-CARBOXYLIC ACID
- H-imidazo[1,2-a]pyridine-8-carboxylic acid
- Imidazo[1,2-a]pyridine-8-...
- 8-imidazo[1,2-a]pyridinecarboxylic acid
- IMidazo[1,2-a]pyridin-8-carboxylic acid
- H-iMidazo[1,2-a]pyridine-8-carbo×ylic acid
- Imidazo[1,2-a]pyridine-8-carboxylicaci
- IMIDAZO[1,2-A]PYRIDINE-8-CARBOXYLIC ACID ISO 9001:2015 REACH
- CAS:
- 133427-08-4
- MF:
- C8H6N2O2
- MW:
- 162.15
- Product Categories:
-
- CHIRAL CHEMICALS
- Mol File:
- 133427-08-4.mol
IMIDAZO[1,2-A]PYRIDINE-8-CARBOXYLIC ACID Chemical Properties
- Density
- 1.41
- storage temp.
- Sealed in dry,Room Temperature
- pka
- -0.61±0.41(Predicted)
- form
- solid
- color
- White
IMIDAZO[1,2-A]PYRIDINE-8-CARBOXYLIC ACID Usage And Synthesis
Synthesis
5345-47-1
7252-83-7
133427-08-4
General procedure for the synthesis of imidazo[1,2-a]pyridine-8-carboxylic acid from 2-aminonicotinic acid and 2-bromo-1,1-dimethoxyethane: To a suspension of 2-aminonicotinic acid (0.69 g, 5.00 mmol) in acetonitrile (20 mL) was added 2-bromo-1,1-dimethoxyethane (0.59 mL, 5.00 mmol). The resulting mixture was heated to 150 °C in a microwave reactor and kept for 2 hours. After completion of the reaction, the precipitate was collected by filtration and washed sequentially with acetonitrile and hexane to afford imidazo[1,2-a]pyridine-8-carboxylic acid (0.924 g) as a gray solid.
References
[1] Patent: WO2009/23253, 2009, A2. Location in patent: Page/Page column 52
[2] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 5, p. 1870 - 1873
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- Imidazo[1,5-a]pyridine-8-carboxylic acid (9CI),H-imidazo[1,5-a]pyridine-8-carboxylic acid
- Imidazo[1,2-a]pyridine-5-carboxylic acid (9CI),H-imidazo[1,2-a]pyridine-5-carboxylic acid
- Imidazo[1,2-a]pyridine-7-carboxylic acid (9CI),H-imidazo[1,2-a]pyridine-7-carboxylic acid
- H-imidazo[1,2-a]pyridine-3-carboxylic acid
- Imidazo[1,2-a]pyridine