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1788-95-0

3-(4-BROMOPHENYL)-2-METHYLQUINAZOLIN-4(3H)-ONE synthesis

9synthesis methods
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Yield:1788-95-0 95.13%

Reaction Conditions:

Stage #1: 2-methyl-4-oxo-3,1-benzoxazine in ethanol at 20; for 0.0833333 h;
Stage #2: 4-bromo-aniline in ethanol at 100; for 6 h;

Steps:

General procedure for synthesis of 2-methyl-3-substituted quinazolin-4(3H)-ones, 8a-q.

General procedure: 2-Methyl-4H-3,1-benzoxazin-4-one, 7 (3.00g, 18.60 mmol) was dissolved in 10 ml of ethanol ina 250 ml round bottom ask and the reaction mixturewas allowed to stir for 5 mins. at room temperature forcomplete dissolution, followed by the addition of thecorresponding amino containing compounds (18.60mmol). The mixture was then heated under reux forthe required number of periods as determined by the TLC monitoring. The reaction mixture was allowedto cool, fltered by suction and air-dried to affordmoderate to excellent yields of various 2-methyl-3-substituted quinazolin-4(3H)-one derivatives, 8a-q.

References:

Ajani, Olayinka O.;Audu, Oluwatosin Y.;Germann, Markus W.;Bello, Babatunde L. [Oriental Journal of Chemistry,2017,vol. 33,# 2,p. 562 - 574]