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Pyrimidine-5-carboxylic acid, 1,2,3,4-tetrahydro-6-methyl-4-(3-pyridyl)-2-thioxo-, ethyl ester synthesis

1synthesis methods
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Yield:123629-47-0 85%

Reaction Conditions:

with ammonium cerium (IV) nitrate in water at 70; for 0.5 h;Biginelli Pyrimidone Synthesis;

Steps:

General procedure for synthesis of pyrimidines 4a-g

General procedure: A mixture of aromatic aldehyde (pyridin-3-carboxaldehydeor thiophen-2-carboxaldehyde) (1mmol), active methylenecompounds (1mmol) namely ethyl acetoacetate, acetylacetoneand 1,3-diphenyl-1,3-propandione, urea dreivatives (urea, thiourea or guanidine hydrochloride) (1mmol), CAN(0.1mmol) in distilled water (10 mL) was heated and stirredunder reflux at 70 °C for 30min. The formed solid productwas filtered, washed with water, dried and recrystallized fromthe proper solvent to give pyrimidines 4a-g.

References:

Salem, Mounir A.;Behalo, Mohamed S.;Elrazaz, Eman [Medicinal Chemistry Research,2019,vol. 28,# 8,p. 1223 - 1234]