Zaprutko, Lucjusz published the artcileRegioselective nitro group substitution. Synthesis of isomeric 4-amino-5-nitro- and 5-amino-4-nitroimidazoles, Computed Properties of 18874-52-7, the main research area is nitroimidazole cyclic amine regioselective nitro group substitution; imidazolamine nitro preparation.
On the basis of the reactions between 4,5-dinitroimidazoles (1-methyl-, 1,2-dimethyl-, and 1-ethoxycarbonylmethyl-4,5-dinitroimidazole) and cyclic amines (morpholine, piperidine, or pyrrolidine) under mild conditions (THF or EtOH solution), the order of nitro group substitution was discovered. The influence of the solvent, steric effects, and the possibility of hydrogen bond formation on the reaction direction was discussed. Also, the mechanism of formation of a diamino substitution product and an interesting isomerization process were presented.
Heterocycles published new progress about Amines, nitro Role: SPN (Synthetic Preparation), PREP (Preparation). 18874-52-7 belongs to class imidazoles-derivatives, name is 5-Bromo-2-methyl-4-nitroimidazole, and the molecular formula is C4H4BrN3O2, Computed Properties of 18874-52-7.
Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem