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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64639Generated: October 24, 2026

Butanoic acid, 2-ethyl-3-oxo-, ethyl ester → 6-ethyl-3,7-dimethyl-5-oxo-5H-thiazolo[3,2-a]pyrimidine-2-carboxylic acid, ethyl ester

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Reaction equation

Participants

RoleNameHCIDCharge
ReactantButanoic acid, 2-ethyl-3-oxo-, ethyl esterHCID 79065—
ReactantEthyl 2-amino-4-methylthiazole-5-carboxylateHCID 343747—
Product6-ethyl-3,7-dimethyl-5-oxo-5H-thiazolo[3,2-a]pyrimidine-2-carboxylic acid, ethyl esterHCID 15590860—

Reaction Conditions

Temperature100 °C

Reaction Steps

2-amino-4-methyl-thiazole-5-carboxylic acid, ethyl ester (10 g) was reacted with ethyl 2-ethyl-acetoacetate (17 g) in polyphosphoric acid (50 g) under stirring at 100° C. for 4 hours. After cooling, dilution with ice water and neutralization with 35% NaOH, the precipitate was filtered, washed with water until neutral and crystallized from hexane to give 6-ethyl-3,7-dimethyl-5-oxo-5H-thiazolo[3,2-a]pyrimidine-2-carboxylic acid, ethyl ester, m.p. 122°-124° C. (9.9 g) which was reacted with N-bromo succinimide (13.75 g) in benzene (260 ml) at the reflux temperature for 11 hours.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04609660
Source datasetuspto-grants-1986_09
ORD IDord-5608d2b5bb544e088bc567ecb14291c5
Source noteuspto-grants-1986_09