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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1778374Generated: November 2, 2026

Trifluoroacetic acid → HCID 68093248, compound

https://huagongshe.com/reaction/1778374

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 66685688HCID 66685688—
SolventDichloromethaneHCID 6344—
ProductHCID 68093248HCID 6809324844.7%

Reaction Steps

TFA (2 mL) was added to a solution of methyl 7-{N-[4-fluoro-2-((Z)-3-{morpholin-4-yl}prop-1-enyl)benzenesulfonyl]-N-(2-trimethylsilanylethoxymethyl)amino]-4H-furo[2,3-c]chromene-6-carboxylate (Intermediate 52, 1.15 g) in DCM (20 mL). The reaction mixture was stirred at room temperature for 30 minutes. Aqueous potassium carbonate was added and the layers were separated. The organic layer was dried (Na2SO4), filtered and the filtrate was concentrated in vacuo. The residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane, with a gradient of 20-80% to give methyl 7-{4-fluoro-2-[(Z)-3-(morpholin-4-yl)prop-1-enyl]benzenesulfonylamino}-4H-furo[2,3-c]chromene-6-carboxylate (0.412 g) as a yellow foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266896B2
Source datasetuspto-grants-2016_02
ORD IDord-26feba33735a426fb80ea4761e362374
Source noteuspto-grants-2016_02