Simple exploration of 4897-25-0

After consulting a lot of data, we found that this compound(4897-25-0)Safety of 5-Chloro-1-methyl-4-nitroimidazole can be used in many types of reactions. And in most cases, this compound has more advantages.

Most of the natural products isolated at present are heterocyclic compounds, so heterocyclic compounds occupy an important position in the research of organic chemistry. A compound: 4897-25-0, is researched, SMILESS is C1=NC(=C(Cl)[N]1C)[N+]([O-])=O, Molecular C4H4ClN3O2Journal, Huaxue Yanjiu Yu Yingyong called A new synthetic technique of 5-chloro-1-methyl-4-nitroimidazole, Author is Liu, Cong; Yan, Xiaofei; Ren, Yingge; Shen, Ning; Liu, Qianfeng, the main research direction is chloro methyl nitroimidazole preparation Azathioprine intermediate.Safety of 5-Chloro-1-methyl-4-nitroimidazole.

A method for the preparation of 5-chloro-1-methyl-4-nitroimidazole was developed with di-Et oxalate, aqueous methylamine formate, phosphorus pentachloride, mixed acid etc as starting materials. The synthesis of the target compound was achieved (64% yield) by a sequence involving an aminolysis reaction, condensation and nitration reaction. The process provided an energy-saving high yield synthetic method (green chem.) and the product thus obtained was confirmed by MS, NMR, FT-IR. The title compound is an intermediate for 6-[(1-methyl-4-nitro-1H-imidazol-5-yl)thio]-9H-purine [Azathioprine, Imuran, immunosuppressant].

After consulting a lot of data, we found that this compound(4897-25-0)Safety of 5-Chloro-1-methyl-4-nitroimidazole can be used in many types of reactions. And in most cases, this compound has more advantages.

Reference:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts