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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874646Generated: October 30, 2026

2-Fluorobenzoyl chloride → N-[5-(5-bromo(2,3-dihydrobenzo[3,4-b]furan-6-yl))(2-pyridyl)](2-fluorophenyl)carboxamide

https://huagongshe.com/reaction/874646

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluorobenzoyl chlorideHCID 9808—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium bicarbonate methylene chlorideHCID 23716255—
Reactant5-(5-Bromo-2,3-dihydrobenzo[3,4-b]furan-6-yl)-2-pyridylamineHCID 58486970—
SolventDichloromethaneHCID 6344—
ProductN-[5-(5-bromo(2,3-dihydrobenzo[3,4-b]furan-6-yl))(2-pyridyl)](2-fluorophenyl)carboxamideHCID 5848693964.9%

Reaction Steps

To a solution of 5-(5-bromo-2,3-dihydrobenzo[3,4-b]furan-6-yl)-2-pyridylamine (139) (13 mg, 0.044 mmol) in 1 ml DCM was added 2-fluorobenzoyl chloride (11 μl, 0.088 mmol) followed by addition of DIEA (38 μl). The resulting solution was stirred at r.t. for overnight. The reaction mixture was worked up with aq. NaHCO3/DCM. DCM phase was washed with brine, concentrated to dryness. The residue was dissolved in 1 ml THF/MeOH/H2O (5:4:1) and stirred with 1N NaOH (100 μl) at r.t. for 2 h and before worked up with EA/aq. NaHCO3. Silica gel flash chromatography furnished N-[5-(5-bromo(2,3-dihydrobenzo[3,4-b]furan-6-yl))(2-pyridyl)](2-fluorophenyl)carboxamide (141) (11 mg, yield: 64.9%, purity>90%) as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08980629B2
Source datasetuspto-grants-2015_03
ORD IDord-b1b707662c624267a2dd5a211acc9581
Source noteuspto-grants-2015_03