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4-[6-(4-methylpiperazin-1-yl)-1H-benzimidazol-2-yl]-2-nitroaniline synthesis

10synthesis methods
1635-61-6 Synthesis
5-Chloro-2-nitroaniline

1635-61-6
295 suppliers
$13.00/25g

4-[6-(4-methylpiperazin-1-yl)-1H-benzimidazol-2-yl]-2-nitroaniline

23623-05-4
7 suppliers
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Yield:-

Steps:

Multi-step reaction with 3 steps
1: 60 percent / K2CO3 / dimethylformamide / 4.5 h / Heating
2: H2 / 10percent Pd/C / methanol / 1.25 h / Ambient temperature
3: 1.171 g / AcOH / 12 h / 55 °C

References:

Harapanhalli;McLaughlin;Howell;Rao;Adelstein;Kassis [Journal of medicinal chemistry,1996,vol. 39,# 24,p. 4804 - 4809]