IMIDAZO[1,2-A]PYRIDINE, 7-BROMO-
IMIDAZO[1,2-A]PYRIDINE, 7-BROMO- Basic information
- Product Name:
- IMIDAZO[1,2-A]PYRIDINE, 7-BROMO-
- Synonyms:
-
- IMIDAZO[1,2-A]PYRIDINE, 7-BROMO-
- 7-Bromoimidazo[1,2-a]pyridine
- 7-bromoH-imidazo[1,2-a]pyridine hydrochloride
- 7-Bromoimidazo[1,2-a]pyri...
- 7-broMoH-iMidazo[1,2-a]pyridine
- 7-bromoimidazo[1,2-a]pyridine HCL
- CAS:
- 808744-34-5
- MF:
- C7H5BrN2
- MW:
- 197.03
- EINECS:
- 1533716-785-6
- Mol File:
- 808744-34-5.mol
IMIDAZO[1,2-A]PYRIDINE, 7-BROMO- Chemical Properties
- Melting point:
- 118-120℃
- Density
- 1.69
- storage temp.
- Sealed in dry,Room Temperature
- form
- solid
- pka
- 5.15±0.50(Predicted)
- color
- White to off-white
- InChI
- InChI=1S/C7H5BrN2/c8-6-1-3-10-4-2-9-7(10)5-6/h1-5H
- InChIKey
- OASOJRLJBDCVNU-UHFFFAOYSA-N
- SMILES
- C12=NC=CN1C=CC(Br)=C2
IMIDAZO[1,2-A]PYRIDINE, 7-BROMO- Usage And Synthesis
Synthesis
107-20-0
84249-14-9
808744-34-5
2-Amino-4-bromopyridine (5.0 g) and 2-chloroacetaldehyde (40% aqueous, 12 mL, 2.5 eq.) were dissolved in anhydrous ethanol (50 mL) and sodium bicarbonate (4.89 g, 2.0 eq.) was added. The reaction mixture was heated to reflux for 6 hours. Upon completion of the reaction, the organic solvent was removed by vacuum rotary evaporation. The residue was extracted with ethyl acetate (60 mL) and washed sequentially with water and saturated saline. The organic layer was dried with anhydrous sodium sulfate, filtered and purified by silica gel column chromatography to afford 7-bromoimidazo[1,2-a]pyridine (4.38 g, 78% yield) as a brown solid.
References
[1] Patent: CN106496222, 2017, A. Location in patent: Paragraph 0095; 0097
[2] Patent: WO2008/124323, 2008, A1. Location in patent: Page/Page column 68
[3] Patent: WO2008/121687, 2008, A2. Location in patent: Page/Page column 53
[4] Patent: WO2017/144633, 2017, A1. Location in patent: Page/Page column 101; 102
[5] Patent: WO2017/144639, 2017, A1. Location in patent: Page/Page column 87
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IMIDAZO[1,2-A]PYRIDINE, 7-BROMO-(808744-34-5)Related Product Information
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