Publication | Closed Access
Synthesis of 4‐aroyl‐5‐nitro‐1<i>H</i>‐imidazoles and 4‐aroyl‐5‐aminoimidazoles
15
Citations
17
References
1986
Year
Combinatorial ChemistryDiversity Oriented SynthesisEngineeringNatural SciencesDiversity-oriented SynthesisOrganic Chemistry‐Nitro‐1 H ‐ImidazolesChemistrySynthesis MethodPharmacologyBiomolecular Engineering
Abstract The reaction of α‐(aryl)‐4‐morpholineacetonitriles (masked aroyl anion equivalents) with N ‐protected 4(5)‐bromo‐5(4)‐nitro‐1 H ‐imidazoles gave 4‐aroyl‐5‐nitroimidazoles which were reduced to afford 4‐aroyl‐5‐aminoimidazoles.
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