Мақола

Structure, aromatic properties and preparation of the quinazolin-4-one molecule

Foziljon SaitkulovTashkent State Agrarian University, st. University, 2, 100140, Tashkent, UzbekistanБ. СапаевTashkent State Agrarian University, st. University, 2, 100140, Tashkent, UzbekistanKhasan NasimovSamarkand State University, st. Hiyoboni University, 140104, Samarkand, UzbekistanDilorom KurbanovaSamarkand State University, st. Hiyoboni University, 140104, Samarkand, UzbekistanNargiza TursunovaSamarkand State University, st. Hiyoboni University, 140104, Samarkand, Uzbekistan

E3S Web of Conferencesjournal2023en

ABI

Аннотация

The government has emphasized the significance of making significant investments in scientific research to develop herbicides, fungicides, bactericides, anthelmintic agents, weed and pest control agents, and alternative pesticides that are eco-friendly and can be exported. In this research, the aromaticity of quinazolin-4-one a and p was studied. A one-stage method for obtaining quinazolin-4-one a was developed by condensation of anthranilic acid and formamide when heated to Wood's alloy. Quinazolin-4-one exhibits conformity with Hückel's rules upon undergoing a reaction with alkali metals, hydrides, and alkalis. An investigation was performed to assess the aromaticity of both para and ortho quinazolin-4-one. Quinazolin-4-one a was obtained through a one-step process, which involved condensing anthranilic acid and formamide using Wood's alloy at a temperature of 130-135 ºС for two hours, which was found to be optimal.

Ҳали таржима қилинмаган

Мавзулар

Quinazolinone synthesis and applications Phenothiazines and Benzothiazines Synthesis and Activities Microwave-Assisted Synthesis and Applications

Идентификаторлар

DOI: 10.1051/e3sconf/202338903075

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