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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1751290Generated: October 28, 2026

Ethyl 3-chloro-3-oxopropionate → N-(5-bromo-3-sulfamoyl-pyridin-2-yl)-malonamic acid ethyl ester

https://huagongshe.com/reaction/1751290

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-chloro-3-oxopropionateHCID 118931—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Amino-5-bromopyridine-3-sulfonamideHCID 52335176—
Solvent1,4-DioxaneHCID 31275—
ProductN-(5-bromo-3-sulfamoyl-pyridin-2-yl)-malonamic acid ethyl esterHCID 5918450369%

Reaction Conditions

Temperature90 °C

Reaction Steps

2-Amino-5-bromo-pyridine-3-sulfonic acid amide (2.5 g, 9.9 mmol) was dissolved in 1,4-dioxane (50 mL). Chlorocarbonyl-acetic acid ethyl ester (1.9 mL, 14.85 mmol) was added and the mixture was heated at 90° C. while stirring for 2 h. Upon cooling to 25° C., the mixture was poured into half-saturated aqueous sodium bicarbonate solution (250 mL). A solid precipitated and was collected by vacuum filtration, rinsed with water (50 mL) and dried in vacuo to afford the desired product, N-(5-bromo-3-sulfamoyl-pyridin-2-yl)-malonamic acid ethyl ester (2.5 g, 6.82 mmol, 69%), as a light beige solid. 1H NMR (400 MHz, DMSO-d6) δ: 1.19 (3H, t, J=7.0 Hz), 3.67 (2H, s), 4.10 (2H, q, J=7.3 Hz), 7.78 (2H, bs), 8.33 (1H, d, J=2.3 Hz), 8.70 (1H, d, J=2.4 Hz), 9.85 (1H, bs).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156832B2
Source datasetuspto-grants-2015_10
ORD IDord-9bbf3092e9484915948afd0748429d94
Source noteuspto-grants-2015_10