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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 637723Generated: October 31, 2026

7-methyl-5-oxo-5H-thiazolo[3,2-a]pyrimidine-2-carboxylic acid, methyl ester → 6-bromo-7-methyl-5-oxo-5H-thiazolo[3,2-a]pyrimidine-2-carboxylic acid, methyl ester

https://huagongshe.com/reaction/637723

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-methyl-5-oxo-5H-thiazolo[3,2-a]pyrimidine-2-carboxylic acid, methyl esterHCID 15590862—
SolventPyridineHCID 1049—
Product6-bromo-7-methyl-5-oxo-5H-thiazolo[3,2-a]pyrimidine-2-carboxylic acid, methyl esterHCID 1559086471.8%

Reaction Steps

7-methyl-5-oxo-5H-thiazolo[3,2-a]pyrimidine-2-carboxylic acid, methyl ester (3.4 g), prepared according to Example 1, was reacted with pyridinium bromide perbromide (5.31 g) in anhydrous pyridine (80 ml) under stirring at room temperature for 40 minutes. The reaction mixture was poured in ice water and the precipitate was filtered and washed with water until neutral. The crude compound was purified over a SiO2 column, using chloroform:ethyl acetate 100:5 as eluent, so obtaining 3.3 g of 6-bromo-7-methyl-5-oxo-5H-thiazolo[3,2-a]pyrimidine-2-carboxylic acid, methyl ester, m.p. 199°-201° C., which was reacted with benzaldehyde (2.3 g) in methanol (90 ml) in the presence of sodium methoxide (0.75 g) under stirring at reflux temperature for 48 hours. The precipitate was filtered and dissolved in a mixture of dimethylformamide and formic acid: the solution was diluted with ice water and the precipitate was filtered and washed with water until neutral. Crystallization from methanol gave 2.4 g of 6-bromo-7-trans-(2-phenyl-ethenyl)-5-oxo-5H-thiazolo[3,2-a]pyrimidine-2-carboxylic acid, m.p. 281°-285° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04558046
Source datasetuspto-grants-1985_12
ORD IDord-bfbb5ad6531440719a4b58e2d4cb572c
Source noteuspto-grants-1985_12