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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2283342Generated: November 2, 2026

Dimethylbarbituric acid → 4-(3-(5-Chloro-6-methoxypyridin-3-yl)phenylsulfonamido)pyridine-3-sulfonamide

https://huagongshe.com/reaction/2283342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylbarbituric acidHCID 69860—
ReactantN,N-diallyl-4-(3-(5-chloro-6-methoxypyridin-3-yl)phenylsulfonamido)pyridine-3-sulfonamideHCID 57750978—
CatalystHCID 178418397HCID 178418397—
SolventDichloromethaneHCID 6344—
Product4-(3-(5-Chloro-6-methoxypyridin-3-yl)phenylsulfonamido)pyridine-3-sulfonamideHCID 5775107949%

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of N,N-diallyl-4-(3-(5-chloro-6-methoxypyridin-3-yl)phenylsulfonamido)pyridine-3-sulfonamide (0.19 g, 0.36 mmol) in dichloromethane (5 mL) was added to tetrakis(triphenylphosphine)palladium(0) (0.021 g, 0.022 mmol) and 1,3-dimethylbarbituric acid (0.336 g, 2.15 mmol) under an atmosphere of argon. The reaction was heated at 100° C. for 15 min in a microwave reactor and the reaction mixture was concentrated. Purification by column chromatography, using chloroform/methanol (95:5-9:1) as the eluent, gave the title compound in 49% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145380B2
Source datasetuspto-grants-2015_09
ORD IDord-a8975695a07944bfb92bdfd10d4d5882
Source noteuspto-grants-2015_09