4-(5-CHLORO-1H-BENZOIMIDAZOL-2-YL)-PHENYLAMINE
4-(5-CHLORO-1H-BENZOIMIDAZOL-2-YL)-PHENYLAMINE Basic information
- Product Name:
- 4-(5-CHLORO-1H-BENZOIMIDAZOL-2-YL)-PHENYLAMINE
- Synonyms:
-
- 4-(5-CHLORO-1H-BENZOIMIDAZOL-2-YL)-PHENYLAMINE
- 4-(5-Chloro-1H-benzo[d]imidazol-2-yl)aniline
- 4-(6-chloro-1h-benzimidazol-2-yl)aniline
- Benzenamine, 4-(6-chloro-1H-benzimidazol-2-yl)-
- CAS:
- 39861-21-7
- MF:
- C13H10ClN3
- MW:
- 243.69
- Mol File:
- Mol File
4-(5-CHLORO-1H-BENZOIMIDAZOL-2-YL)-PHENYLAMINE Chemical Properties
- storage temp.
- 2-8°C(protect from light)
- Appearance
- Light yellow to brown Solid
Safety Information
- Hazard Codes
- Xi
- HazardClass
- IRRITANT
4-(5-CHLORO-1H-BENZOIMIDAZOL-2-YL)-PHENYLAMINE Usage And Synthesis
Synthesis
150-13-0
95-83-0
39861-21-7
General procedure for the synthesis of 4-(5-chloro-1H-benzo[d]imidazol-2-yl)aniline from p-aminobenzoic acid and 4-chloro-1,2-benzenediamine: Eaton's reagent (10% v/v (w/v)) was added drop-wise to a mixture of 4-chloro-1,2-benzenediamine (1 equiv) and p-aminobenzoic acid (1 equiv). Subsequently, the reaction mixture was heated at 130 °C for 5-6 h. The reaction process was monitored by TLC and LCMS. After completion of the reaction, the mixture was cooled to room temperature and neutralized with 10% sodium hydroxide solution to pH 6-7. The precipitate formed was collected by filtration and washed repeatedly with water and subsequently dried. Finally, the resulting solid was purified by ethanol recrystallization to afford the target product 4-(5-chloro-1H-benzo[d]imidazol-2-yl)aniline in good yield.
References
[1] Bioorganic and Medicinal Chemistry, 2014, vol. 22, # 21, p. 5970 - 5987
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