18773-95-0Relevant articles and documents
Effect of the Leaving Group in the Hydrolysis of N-Acylimidazoles. The Hydroxide Ion, Water, and General Base Catalyzed Hydrolysis of N-Acyl-4(5)-nitroimidazoles
Fife, Thomas H.,Natarajan, R.,Werner, Milton H.
, p. 740 - 746 (1987)
The second-order rate constants kOH for hydroxide ion catalyzed hydrolysis of N-acylimidazoles substituted in the imidazole group show only a moderate dependence on the pKa of the leaving group (βlg = -0.28), which indicat
Synthesis of Some Benzimidazole-based Heterocycles and their Application as Copper Corrosion Inhibitors
Eldebss, Taha M. A.,Farag, Ahmad M.,Shamy, Adel Y. M.
, p. 371 - 390 (2019/01/08)
A series of new substituted benzimidazoles embedded with a variety of function groups has been synthesized from N-methyl-2-bromoacetylbenzimidazole. The synthesized compounds were fully characterized, and their structures were elucidated based on elemental analysis, spectral data, and alternative synthetic pathways, whenever possible. Some of benzimidazole derivatives were tested as corrosion inhibitors.
A azole amide preparation method of the compound
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Paragraph 0019-0021; 0025-0027; 0065-0066, (2018/04/27)
A preparation method of an azole-series amide compound. The invention discloses a method including a reaction that the azole-series amide is synthesized from a carboxylic acid compound and an azole compound with a copper salt as a catalyst and molecular o