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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272223Generated: November 1, 2026

2-Fluorobenzoyl chloride → HCID 58486713, compound

https://huagongshe.com/reaction/2272223

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluorobenzoyl chlorideHCID 9808—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium bicarbonate methylene chlorideHCID 23716255—
ReactantHCID 58486925HCID 58486925—
SolventDichloromethaneHCID 6344—
ProductHCID 58486713HCID 5848671366.4%

Reaction Steps

To a solution of 5-(5-chloro-2,3-dihydrobenzo[3,4-b]furan-6-yl)-2-pyridylamine (151) (15 mg, 0.06 mmol) in 1 ml DCM was added 2-fluorobenzoyl chloride (11 μl, 0.088 mmol) followed by addition of DIEA (52 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 (120 μl) at r.t. for 2 h and before worked up with EA/aq. NaHCO3. Silica gel flash chromatography furnished N-[5-(5-chloro(2,3-dihydrobenzo[3,4-b]furan-6-yl))(2-pyridyl)](2-fluorophenyl)carboxamide (153) (14.7 mg, yield: 66.4%, purity>90%) as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120751B2
Source datasetuspto-grants-2015_09
ORD IDord-6fd1d99291e0402caf4312148590d6b5
Source noteuspto-grants-2015_09