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3-ALLYL-2-MERCAPTO-3H-QUINAZOLIN-4-ONE synthesis

9synthesis methods
-

Yield:21263-59-2 92%

Reaction Conditions:

with carbon disulfide;potassium hydroxide in ethanol; for 3 h;Reflux;

Steps:

General Experimental Procedure for 2-thioxo- 2,3-dihydroquinazolin-4(1H)-one derivatives

General procedure: A solution of isatoic anhydride (1 mmol) and appropriate amine (1 mmol) in 10 ml EtOH was stirred at reflux for 3 h. Then, a mix- ture of carbon disulfide (2 mmol) and KOH (1 mmol) was added to the reaction mixture and stirring continued under the same condi- tions for 3 h. The reaction mixture was cooled to room tempera- ture and poured into 20 ml water. The precipitate was collected by filtration, washed with water, and recrystallized using EtOH to give desirable product as colorless crystals.

References:

Adibi, Hossein;Asgari, Mohammad Sadegh;Attarroshan, Mahshid;Farid, Sara Moghadam;Hamedifar, Haleh;Hosseini, Samanesadat;Iraji, Aida;Kabiri, Maryam;Khoshneviszadeh, Mehdi;Larijani, Bagher;Mahdavi, Mohammad;Moayedi, Seyedeh Sara;Moazzam, Ali;Pirhadi, Somayeh;Sakhteman, AmirHossein;Sepehri, Nima [Journal of Molecular Structure,2022,vol. 1253,art. no. 132283]

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