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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272293Generated: November 1, 2026

Potassium Carbonate → HCID 131732257, compound

https://huagongshe.com/reaction/2272293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-4-fluoro-1-nitrobenzeneHCID 75017—
ReactantHCID 67352455HCID 67352455—
SolventWater 1,2-dimethoxyethaneHCID 18180031—
ProductHCID 131732257HCID 13173225765%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 2-(4-chlorophenyl)-5-cyclopropyl-N-methyl-6-(methylsulfonamido)benzofuran-3-carboxamide (2.00 g, 4.77 mmol), 2-chloro-4-fluoronitrobenzene (1.68 g, 9.55 mmol), and potassium carbonate (1.98 g, 14.3 mmol) in 4:1 DME/water (20 mL) in a sealed vessel was heated to 100° C. with stirring. After 18 hours the mixture was treated with an additional 2.00 g portion of potassium carbonate, heated at 100° C. for another 15 hours, and then stirred at RT for 3 days. The mixture was partitioned between EtOAc and water. After separating the phases, the aqueous portion was extracted with two additional portions of EtOAc. The combined EtOAc solutions were washed with water (2×), brine (1×), dried over sodium sulfate and concentrated to dryness at reduced pressure. The crude material was subjected to flash chromatography (silica gel, gradient from DCM to 7:3 DCM/EtOAc) to afford a tacky, yellow foam. This material was crystallized from hexane/EtOAc to give the title compound (1.78 g, 65%) as a light yellow solid. LCMS (m/z, ES+)=574 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09119868B2
Source datasetuspto-grants-2015_09
ORD IDord-693b998adab946c499e599d328a8a065
Source noteuspto-grants-2015_09