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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1755160Generated: November 4, 2026

Ethanol → 4-{[(4-Benzofuran-2-yl-phenylcarbamoyl)-(4-tert-butyl-phenyl)-methyl]-amino}benzoic Acid

https://huagongshe.com/reaction/1755160

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium CarbonateHCID 10340—
ReactantBenzo[b]furan-2-boronic acidHCID 2776266—
Reactant4-{[(4-tert-Butyl-phenyl)-(4-iodo-phenylcarbamoyl)-methyl]-amino}-benzoic AcidHCID 67486727—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product4-{[(4-Benzofuran-2-yl-phenylcarbamoyl)-(4-tert-butyl-phenyl)-methyl]-amino}benzoic AcidHCID 67486468100%

Reaction Steps

4-{[(4-tert-Butyl-phenyl)-(4-iodo-phenylcarbamoyl)-methyl]-amino}-benzoic acid acid (340 mg, 0.6 mmol) was taken up in 8 mL of DME, 4 mL of ethanol and 2 mL of water. Na2CO3 (254 mg, 2.4 mmol), PdCl2(O-tolyl)2 (61 mg, 0.0078 mmol) and benzo[B]furan-2-boronic acid (194 mg, 1.2 mmol) were then added, flushed with nitrogen and heated to reflux for 1 h. Cooled to RT, EtOAc (20 mL) was added and extracted with water (20 mL). The organic layer was washed again with water (20 mL), dried over sodium sulfate, filtered and the organic layer was removed under reduced pressure to give a white solid (120 mg, 100%). 1H NMR showed the compound to be very clean and sufficient for the following step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169201B2
Source datasetuspto-grants-2015_10
ORD IDord-823e890649874919895b696589ea24cb
Source noteuspto-grants-2015_10