2-(1,7-diazabicyclo[4.3.0]nona-2,4,6,8-tetraen-8-yl)acetic acid
2-(1,7-diazabicyclo[4.3.0]nona-2,4,6,8-tetraen-8-yl)acetic acid Basic information
- Product Name:
- 2-(1,7-diazabicyclo[4.3.0]nona-2,4,6,8-tetraen-8-yl)acetic acid
- Synonyms:
-
- Imidazo[1,2-a]pyridin-2-acetic acid
- Imidazo[1,2-a]pyridine-2-acetic acid
- imidazol[1,2-A]pyridin-2-yl-acetic acid
- Minodronic Impurity 2
- 2-(1,7-diazabicyclo[4.3.0]nona-2,4,6,8-tetraen-8-yl)acetic acid
- IMIDAZO[1,2-A]PYRIDIN-2-YLACETIC ACID HYDROCHLORIDE
- Nsc296220
- Minodronic Acid Impurity 29
- CAS:
- 19741-30-1
- MF:
- C9H8N2O2
- MW:
- 176.17
- Mol File:
- 19741-30-1.mol
2-(1,7-diazabicyclo[4.3.0]nona-2,4,6,8-tetraen-8-yl)acetic acid Chemical Properties
- Melting point:
- 207-208 °C(Solv: ethanol (64-17-5); water (7732-18-5))
- Density
- 1.35±0.1 g/cm3(Predicted)
- storage temp.
- 2-8°C
- form
- solid
- pka
- 1.91±0.10(Predicted)
2-(1,7-diazabicyclo[4.3.0]nona-2,4,6,8-tetraen-8-yl)acetic acid Usage And Synthesis
Uses
2-{imidazo[1,2-a]pyridin-2-yl}acetic acid is a useful research chemical.
Synthesis
504-29-0
27807-84-7
19741-30-1
The general procedure for the synthesis of 2-(imidazo[1,2-a]pyridin-2-yl)acetic acid from 2-aminopyridine (20 g, 212 mmol) and ethyl 4-chloro-3-oxobutanoate (28.7 mL, 212 mmol) is as follows: firstly, 2-aminopyridine was added to 300 mL of ethanol, followed by the addition to a reaction vessel containing a magnetic stir bar of 4-chloro-3- ethyl oxobutyrate. The reaction mixture was stirred at 80°C for 20 hours. Upon completion of the reaction, the ethanol was evaporated and the crude product was dissolved in 100 mL of 0.5 N hydrochloric acid. The aqueous phase was extracted three times with 50 mL of dichloromethane to remove organic impurities. The product was retained in the aqueous phase and 37 g of crude product was obtained by concentration under reduced pressure. The crude product was purified by silica gel chromatography using a dichloromethane/methanol gradient elution (yield: 8.3 g, 19% yield). The resulting ester was dissolved in 200 mL of methanol and 7 mL of 10 M sodium hydroxide solution was added. The reaction mixture was stirred at room temperature for 12 h until the ester was completely saponified. After evaporation of methanol, the aqueous phase was acidified to pH=7. The precipitated product was filtered and washed with ether (yield: 7.6 g, 99%).LCMS (Method 1): retention time (Rt) = 0.435 min; HRMS (ESIpos): m/z [M + H]+ C9H8N2O2 Calculated value 177.0659, measured value 177.0660.
References
[1] Patent: EP3275885, 2018, A1. Location in patent: Paragraph 0118; 0119
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2-(1,7-diazabicyclo[4.3.0]nona-2,4,6,8-tetraen-8-yl)acetic acid(19741-30-1)Related Product Information
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- IMIDAZO[1,2-A]PYRIDIN-2-YL-METHYLAMINE DIHYDROCHLORIDE
- Imidazo[1,2-a]pyridin-2-yl-methylamine dihydrochloride
- ETHYL TRANS-4-OXO-2-BUTENOATE
- IMidazo[1,2-a]pyridine-3-aceticacid,ethylester
- IMIDAZO[1,2-A]PYRIDIN-3-YL-ACETIC ACID
- fumaraldehydic acid
- Imidazo[1,5-a]pyridine-5-carboxaldehyde (9CI)
- Imidazo[1,2-a]pyridine-6-carbaldehyde
- H-imidazo[1,5-a]pyridine-5-carboxylic acid
- Methyl iMidazo[1,5-a]pyridine-8-carboxylate
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- Imidazo[1,2-a]pyrazin-3-ylamine
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