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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 637722Generated: October 31, 2026

Sulfuryl chloride → HCID 15590863, compound

https://huagongshe.com/reaction/637722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuryl chlorideHCID 24648—
ReactantSodium BicarbonateHCID 516892—
Reactant7-methyl-5-oxo-5H-thiazolo[3,2-a]pyrimidine-2-carboxylic acid, methyl esterHCID 15590862—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 15590863HCID 1559086367.5%

Reaction Steps

7-methyl-5-oxo-5H-thiazolo[3,2-a]pyrimidine-2-carboxylic acid, methyl ester (5.5 g; m.p. 146°-148° C.), prepared according to Example 1, was reacted with sulfuryl chloride (3.6 g) in dichloroethane (150 ml) under stirring at room temperature for 30 minutes. The reaction mixture was poured into ice water containing NaHCO3 : the organic phase was separated and evaporated in vacuo to dryness: crystallization from methanol gave 6-chloro-7-methyl-5-oxo-5H-thiazolo[3,2-a]pyrimidine-2-carboxylic acid, methyl ester (4.28 g), m.p. 218°-220° C., which was reacted with benzaldehyde (3.5 g) in methanol (150 ml) in the presence of sodium methoxide (2.68 g) under stirring at reflux temperature for 24 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 CH2Cl2 -methanol gave 3.1 g of 6 -chloro-7-trans-(2-phenyl-ethenyl)-5-oxo-5H-thiazolo[3,2-a]pyrimidine-2-carboxylic acid, m.p. 265°-270° C. dec.,

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04558046
Source datasetuspto-grants-1985_12
ORD IDord-94f9e895b18b476c94065a26a163d378
Source noteuspto-grants-1985_12