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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272219Generated: November 1, 2026

2-Fluorobenzoyl chloride → HCID 58486919, compound

https://huagongshe.com/reaction/2272219

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluorobenzoyl chlorideHCID 9808—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium bicarbonate methylene chlorideHCID 23716255—
Reactant5-(6-Chloro-2,3-dihydro-5-benzofuranyl)-2-pyridinamineHCID 58486702—
SolventDichloromethaneHCID 6344—
ProductHCID 58486919HCID 5848691945.8%

Reaction Steps

To a solution of 5-(6-chloro-2,3-dihydrobenzo[3,4-b]furan-5-yl)-2-pyridylamine (144) (19 mg, 0.045 mmol) in 1 ml DCM was added 2-fluorobenzoyl chloride (16 μl, 3 eq) followed by addition of DIEA (39 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. Prep HPLC purification furnished N-[5-(6-chloro(2,3-dihydrobenzo[3,4-b]furan-5-yl))(2-pyridyl)](2-fluorophenyl)carboxamide (146) (7.6 mg, yield: 45.8%, purity>95%) as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120751B2
Source datasetuspto-grants-2015_09
ORD IDord-6f0090c8897c44eabd9e8eeb8ed0330e
Source noteuspto-grants-2015_09