Basic information Safety Supplier Related

Imidazo[1,2-a]pyridin-6-amine (9CI)

Basic information Safety Supplier Related

Imidazo[1,2-a]pyridin-6-amine (9CI) Basic information

Product Name:
Imidazo[1,2-a]pyridin-6-amine (9CI)
Synonyms:
  • Imidazo[1,2-a]pyridin-6-amine (9CI)
  • Imidazo[1,2-a]pyridin-6-amine
  • H-imidazo[1,2-a]pyridin-6-amine
  • Imidazo[1,2-a]pyridin-6-amine[N/A
CAS:
235106-53-3
MF:
C7H7N3
MW:
133.15
Product Categories:
  • Building Blocks
  • Imidazo[x,x-y]pyridine
  • AMINETERTIARY
Mol File:
235106-53-3.mol
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Imidazo[1,2-a]pyridin-6-amine (9CI) Chemical Properties

Density 
1.32±0.1 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
pka
7.50±0.50(Predicted)
Appearance
Light brown to black Solid
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Safety Information

HS Code 
2933399990
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Imidazo[1,2-a]pyridin-6-amine (9CI) Usage And Synthesis

Synthesis

25045-82-3

235106-53-3

At room temperature and atmospheric pressure, 600 mg (3.68 mmol) of 6-nitroimidazo[1,2-a]pyridine was dissolved in 30 mL of ethanol and 60 mg of palladium/carbon catalyst (10% palladium loading) was added. The reaction system was placed in a hydrogen atmosphere and the reaction was stirred overnight. Upon completion of the reaction, the catalyst was removed by filtration through a diatomaceous earth pad and the filter cake was washed with ethanol. The filtrate and washings were combined and concentrated under reduced pressure to remove the solvent to give the crude product 6-aminoimidazo[1,2-a]pyridine, which can be used in subsequent reactions without further purification. Yield: 512 mg (quantitative yield). The product was analyzed by LC/MS [Method 5]: retention time Rt = 0.89 min; mass spectrum (ESI positive ion mode): m/z = 134 ([M+H]+). 1H-NMR (400 MHz, DMSO-d6) chemical shift δ [ppm]: 7.72-7.62 (m, 2H), 7.33 (d, 1H), 7.30 (d, 1H) , 6.80 (dd, 1H), 4.83 (s, 2H).

References

[1] Patent: US2017/275282, 2017, A1. Location in patent: Paragraph 0507-0509
[2] Patent: WO2009/122180, 2009, A1. Location in patent: Page/Page column 105
[3] Yakugaku Zasshi, 1949, vol. 69, p. 496
[4] Chem.Abstr., 1950, p. 4474
[5] Patent: US2016/272637, 2016, A1. Location in patent: Paragraph 0511; 0512; 0513; 0514

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