Basic information Safety Supplier Related

2,5,6-TRICHLORO-1H-BENZIMIDAZOLE

Basic information Safety Supplier Related

2,5,6-TRICHLORO-1H-BENZIMIDAZOLE Basic information

Product Name:
2,5,6-TRICHLORO-1H-BENZIMIDAZOLE
Synonyms:
  • 2,5,6-trichloro-1H-benzo[d]imidazole
  • 2,5,6-trichloro-1H-1,3-benzodiazole
  • Benzimidazole, 2,5,6-trichloro-
  • 2,5,6-TRICHLORO-1H-BENZIMIDAZOLE
  • 1H-Benzimidazole, 2,5,6-trichloro-
  • 2,5,6-Trichlorobenzimidazole
  • 2,5,6-trichloro-3aH-benzimidazole
  • MaribavirIntermediate
CAS:
16865-11-5
MF:
C7H3Cl3N2
MW:
221.47
Mol File:
16865-11-5.mol
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2,5,6-TRICHLORO-1H-BENZIMIDAZOLE Chemical Properties

Boiling point:
399.3±45.0 °C(Predicted)
Density 
1.691±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
6.87±0.10(Predicted)
Appearance
Off-white to yellow Solid
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2,5,6-TRICHLORO-1H-BENZIMIDAZOLE Usage And Synthesis

Uses

2,5,6-Trichlorobenzimidazole has been used in the synthesis of trihaloribofuranosylbenzimidazole derivatives with antiviral activity.

Synthesis

2033-29-6

16865-11-5

The general procedure for the synthesis of 2,5,6-trichlorobenzimidazole using 5,6-dichloro-1H-benzo[d]imidazol-2(3H)-one as starting material was as follows: completely dry 5,6-dichloro-1,3-dihydro-benzimidazol-2-one (28.4 g, 0.14 mol) was suspended in trichlorophosphorus (POCl3, 75 mL). The reaction mixture was heated to reflux temperature, kept for 3 h and then cooled to room temperature. The reaction solution was slowly poured into crushed ice/water mixture (1.5 L) under vigorous stirring. The pH of the mixture was adjusted with sodium hydroxide (NaOH) solution to 7.0. The precipitated solid product was collected by filtration, washed with water and dried to afford 2,5,6-trichlorobenzimidazole (27.9 g, 90% yield). The crude product obtained can be used directly in the subsequent reaction without further purification.

References

[1] Patent: WO2009/134750, 2009, A1. Location in patent: Page/Page column 60
[2] Journal of Medicinal Chemistry, 2016, vol. 59, # 15, p. 7188 - 7211
[3] Patent: WO2011/23812, 2011, A1. Location in patent: Page/Page column 69
[4] Patent: WO2012/117062, 2012, A1. Location in patent: Page/Page column 29
[5] Journal of Medicinal Chemistry, 1997, vol. 40, # 4, p. 586 - 593

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