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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243055Generated: November 1, 2026

Dimethylamine → Ethyl 2-Chloro-4-dimethylcarbamoyl-thiazole-5-carboxylate

https://huagongshe.com/reaction/2243055

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
Reactant2,6-LutidineHCID 7937—
ReactantOxalyl chlorideHCID 65578—
Reactant2-Chloro-5-(ethoxycarbonyl)-1,3-thiazole-4-carboxylic acidHCID 59208347—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductEthyl 2-Chloro-4-dimethylcarbamoyl-thiazole-5-carboxylateHCID 5920839776%

Reaction Conditions

Temperature45 °C

Reaction Steps

To a stirred solution of 2-chloro-5 (ethoxy carbonyl)-1,3-thiazole-4-carboxylic acid (Intermediate 7, 2 g, 8.01 mmol) in dry dichloromethane (20 mL) was added oxalyl chloride (1.37 mL, 16.02 mmol) and 2 drops of dry dimethylformamide. The reaction mixture was heated to 45° C. for 90 minutes. After the completion of the reaction, the reaction mixture was evaporated to dryness under reduced pressure. The residue was dissolved in dry dichloromethane (20 mL) and was cooled to 0° C., then 2,6-lutidine (0.97 mL, 8.4 mmol) was added followed by addition of N,N-dimethylamine (2 M solution in tetra hydro furan, 4.19 mL, 8.4 mmol). After completion of the reaction, the reaction mixture was concentrated to dryness and the residue was extracted with ethyl acetate (2×50 mL). The organic layer was washed with 1 N hydrochloric acid, water and brine (1×50 mL), and concentrated after drying over anhydrous sodium sulfate to afford 1.6 g (72.7%) of the title compound as a thick syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674801B2
Source datasetuspto-grants-2010_03
ORD IDord-a045682d867f43f092cd74971b0872bd
Source noteuspto-grants-2010_03