Machine Learning in Chemistry about 4531-54-8

After consulting a lot of data, we found that this compound(4531-54-8)Application In Synthesis of 1-Methyl-4-nitro-1H-imidazol-5-amine can be used in many types of reactions. And in most cases, this compound has more advantages.

The chemical properties of alicyclic heterocycles are similar to those of the corresponding chain compounds. Compound: 1-Methyl-4-nitro-1H-imidazol-5-amine, is researched, Molecular C4H6N4O2, CAS is 4531-54-8, about Nucleophilic substitution reactions of 1-methyl-4,5-dinitroimidazole with aqueous ammonia or sodium azide, the main research direction is nucleophilic substitution reaction methyldinitroimidazole aqueous ammonia sodium azide.Application In Synthesis of 1-Methyl-4-nitro-1H-imidazol-5-amine.

In this work, 5-amino-1-methyl-4-nitroimidazole was synthesized by amination reaction of 1-methyl-4,5-dinitroimidazole with aqueous ammonia in 95% yield. Meanwhile, one of its isomers, 4-amino-1-methyl-5-nitroimidazole as byproduct was obtained from the filtrate. Furthermore, nucleophilic substitution reaction of 1-methyl-4,5-dinitroimidazole with sodium azide gave 5-azido-1-methyl-4-nitroimidazole in 98% yield. The three compounds were characterized by IR, 1H and 13C NMR spectra, m.ps., and elemental anal. The structure of 4-amino-1-methyl-5-nitroimidazole was further confirmed by single crystal X-ray diffraction. These reactions indicate that the nitro group at position 5 of 1-methyl-4,5-dinitroimidazole is quite unstable, as well as partial substitution of nitro group at position 4 also occurred in aqueous ammonia. Only one nitro group of the two is involved in nucleophilic substitution reaction in each case.

After consulting a lot of data, we found that this compound(4531-54-8)Application In Synthesis of 1-Methyl-4-nitro-1H-imidazol-5-amine can be used in many types of reactions. And in most cases, this compound has more advantages.

Reference:
Thiomorpholine – Wikipedia,
Thiomorpholine | C4H9NS – PubChem