Basic information Safety Supplier Related

4-Iodo-1H-indazol-3-ylamine

Basic information Safety Supplier Related

4-Iodo-1H-indazol-3-ylamine Basic information

Product Name:
4-Iodo-1H-indazol-3-ylamine
Synonyms:
  • 3-Amino-4-iodo-1H-indazole
  • 4-Iodo-1H-indazol-3-ylamine
  • 3-Amino-4-iodo-1H-indazol...
  • 1H-Indazol-3-aMine, 4-iodo-
  • 3-Amino-4-iodoindazole
  • 4-iodo-1H-indazol-3-amine
  • 4-iodo-1H-indazol-4-amine
  • 4-l0d0-1H-indazol-3-amine
CAS:
599191-73-8
MF:
C7H6IN3
MW:
259.05
Mol File:
599191-73-8.mol
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4-Iodo-1H-indazol-3-ylamine Chemical Properties

Melting point:
154-155°
Boiling point:
452.2±25.0 °C(Predicted)
Density 
2.168±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
form 
Crystalline Solid
pka
13.85±0.40(Predicted)
color 
Off-white to brown
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Safety Information

HazardClass 
IRRITANT
HS Code 
29339980
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4-Iodo-1H-indazol-3-ylamine Usage And Synthesis

Synthesis

79544-29-9

599191-73-8

General procedure for the synthesis of 3-amino-4-iodoindazole from 2-fluoro-6-iodobenzonitrile: 500 mg of 2-fluoro-6-iodobenzonitrile and 1.3 ml of 85% hydrazine hydrate were dissolved in 10 ml of n-butanol and heated to 110 °C. The reaction mixture was stirred for 6 hours and then cooled to room temperature. Liquid-liquid separation was carried out by adding water and ethyl acetate. The aqueous phase was extracted with ethyl acetate and the combined organic phases were washed with saturated sodium chloride solution, dried over anhydrous sodium sulfate, filtered and concentrated to give 502 mg of 4-iodo-1H-indazol-3-amine as a brown solid in 96% yield.1H NMR (300 MHz, DMSO-d6) δ (ppm): 5.05 (s, 2H), 6.90-6.96 (m, 1H), 7.29 (d, J = 8.1 Hz, 1H), 7.34 (d, J = 7.5 Hz, 1H), 11.80 (s, 1H).

References

[1] ACS Medicinal Chemistry Letters, 2014, vol. 5, # 5, p. 592 - 597
[2] Patent: EP3112351, 2017, A1. Location in patent: Paragraph 0029
[3] Organic Process Research and Development, 2009, vol. 13, # 6, p. 1419 - 1425
[4] European Journal of Medicinal Chemistry, 2015, vol. 104, p. 139 - 147
[5] Journal of Medicinal Chemistry, 2007, vol. 50, # 7, p. 1584 - 1597

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