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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428199Generated: November 1, 2026

Sodium Carbonate → 1-Ethyl-3-[3-(3-hydroxy-phenyl)-pyrido[2,3-b]pyrazine-6-yl]-urea

https://huagongshe.com/reaction/1428199

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant(3-hydroxyphenyl)boronic AcidHCID 2734359—
ReactantN,N-Dimethylformamide--water (1/1)HCID 21962138—
Reactant1-(3-Chloropyrido[2,3-b]pyrazin-6-yl)-3-ethylureaHCID 58881791—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product1-Ethyl-3-[3-(3-hydroxy-phenyl)-pyrido[2,3-b]pyrazine-6-yl]-ureaHCID 58881893—

Reaction Conditions

Temperature90 °C

Reaction Steps

100 mg 1-(3-chloropyrido[2,3-b]pyrazine-6-yl)-3-ethyl-urea (0.40 mmol) was presented in a dimethylformamide/water mixture under nitrogen as protective gas. Then 60.3 mg 3-hydroxyphenyl boronic acid (0.44 mmol), 126 mg sodium carbonate (1.19 mmol) and 23 mg tetrakis(triphenylphosphine) palladium(0) (0.02 mmol) were added. The reaction mixture was stirred at 90° C. for 4 hours. The mixture was filled with water for reprocessing and the deposited solid rewashed with dichloromethane. The resulting raw product was stirred again in warm DCM, filtered off and dried. A yellow solid was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937068B2
Source datasetuspto-grants-2015_01
ORD IDord-cb0db14be6bb48ee917625a45bc9980f
Source noteuspto-grants-2015_01