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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1353003Generated: October 31, 2026

Ethyl bromopyruvate → HCID 11795549, compound

https://huagongshe.com/reaction/1353003

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromopyruvateHCID 66144—
ReactantSodium BicarbonateHCID 516892—
Reactant4-chloro-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamideHCID 178504796—
SolventIsopropanolHCID 3776—
ProductHCID 11795549HCID 11795549—

Reaction Steps

A mixture of 4-chloro-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamide (Example 1, step 1) (12.1 g, 39.2 mmol), sodium bicarbonate (6.58 g, 78.3 mmol), and 90% ethyl bromopyruvate (16.9 g) in 480 ml of 2-propanol was stirred at reflux overnight. After cooling, the mixture was concentrated. The residue was partitioned between dichloromethane and water and the aqueous layer further extracted with dichloromethane. The combined organic extracts were dried over sodium sulfate, filtered, and evaporated. Trituration of the residue with ethyl acetate gave the title compound as a pale beige, crystalline solid (6.61 g): mp (DSC) 218° C. Anal. Calc'd. for C19H17ClN2O4S (MW 404.87): C, 56.37; H, 4.23; N, 6.92. Found: C, 56.28;.H, 4.13; N, 6.80.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07220770B2
Source datasetuspto-grants-2007_05
ORD IDord-7f8785cbeea94ec7b52a1be6403aaa3c
Source noteuspto-grants-2007_05