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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595653Generated: October 29, 2026

2,4-Difluoro-1-iodobenzene → 6-amino-5-bromo-2-(2,4-difluorophenyl)-N-methylbenzofuran-3-carboxamide

https://huagongshe.com/reaction/595653

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Difluoro-1-iodobenzeneHCID 137519—
Reactant(6-Amino-5-bromo-3-(methylcarbamoyl)benzofuran-2-yl)boronic acidHCID 90332513—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventDimethylformamideHCID 6228—
Product6-amino-5-bromo-2-(2,4-difluorophenyl)-N-methylbenzofuran-3-carboxamideHCID 9033247670.5%

Reaction Conditions

Temperature15 °C

Reaction Steps

To a mixture of (6-amino-5-bromo-3-(methylcarbamoyl)benzofuran-2-yl)boronic acid (4.78 g, 11.46 mmol), K3PO4.3H2O (8.32 g, 31.25 mmol) and 2,4-difluoro-1-iodobenzene (2.50 g, 10.42 mmol) in DMF (25 mL) was added Pd(dppf)Cl2 (380 mg, 0.52 mmol) under N2, and then the mixture was stirred at 15° C. for 3 hours. After the solvent was removed, EtOAc/H2O (10 mL/20 mL) was added to the mixture. After stirring 15 minutes, the resulting solid was filtered to give the product of 6-amino-5-bromo-2-(2,4-difluorophenyl)-N-methylbenzofuran-3-carboxamide (2.80 g, yield: 70%). 1H-NMR (DMSO-d6, 400 MHz) δ 8.06 (d, J=1.6 Hz, 1H), 7.74 (d, J=10.4 Hz, 1H), 7.70 (s, 1H), 7.41 (s, 1H), 7.24 (s, 1H), 7.00 (s, 1H), 5.58 (br s, 2H), 2.76 (s, 3H). MS (M+H)+: 281/283

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09243002B2
Source datasetuspto-grants-2016_01
ORD IDord-95cb501410ad4f28881291adcb92963a
Source noteuspto-grants-2016_01