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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504406Generated: November 4, 2026

Cesium carbonate → (E)-ethyl 3-(5-(benzylthio)-2-((3'-chloro-3-fluoro-5-methoxy-[1,1'-biphenyl]-4-yl)amino)phenyl)acrylate

https://huagongshe.com/reaction/1504406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant3'-Chloro-3-fluoro-4-iodo-5-methoxy-1,1'-biphenylHCID 117737022—
Reactant(E)-Ethyl 3-(2-amino-5-(benzylthio)phenyl)acrylateHCID 117740420—
Catalyst1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Product(E)-ethyl 3-(5-(benzylthio)-2-((3'-chloro-3-fluoro-5-methoxy-[1,1'-biphenyl]-4-yl)amino)phenyl)acrylateHCID 11774685753.8%

Reaction Steps

A pressure vessel was charged with (E)-ethyl 3-(2-amino-5-(benzylthio)phenyl)acrylate (497.91 mg, 1.589 mmol, made via Method 42, Steps 1-2), 3′-chloro-3-fluoro-4-iodo-5-methoxy-1,1′-biphenyl (605 mg, 1.668 mmol), Xantphos (46.0 mg, 0.079 mmol), Pd2(dba)3 (36.4 mg, 0.040 mmol), and cesium carbonate (1035 mg, 3.18 mmol) were added. The vessel was flushed with Ar (g), then toluene (3177 μl) was added. The vessel was sealed and lowered into a 110° C. heating bath for 4 h. The heating bath was turned off, and the vessel was allowed to cool to RT with the bath. In the morning, the mixture was filtered through celite. The filter pad was washed with EtOAc (3×). The filtrate was concentrated. The residue was purified by chromatography on silica gel (40-g Redi-Sep Gold column, 0-30% EtOAc/Heptane with 5% DCM) to give (E)-ethyl 3-(5-(benzylthio)-2-((3′-chloro-3-fluoro-5-methoxy-[1,1′-biphenyl]-4-yl)amino)phenyl)acrylate (468.1 mg, 0.854 mmol, 53.8% yield) as a yellow solid. m/z (ESI) 548.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212182B2
Source datasetuspto-grants-2015_12
ORD IDord-522e64c23b27447286deb6416be964d5
Source noteuspto-grants-2015_12