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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335878Generated: October 30, 2026

Diethylamine → HCID 86658475, compound

https://huagongshe.com/reaction/335878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethylamineHCID 8021—
ReactantHCID 86658476HCID 86658476—
SolventDichloromethaneHCID 6344—
ProductHCID 86658475HCID 86658475—

Reaction Steps

(N,N,N′,N′-tetramethyl-o-(1H-benzotriazol-1-yl)uronium tetrafluoroborate (53.1 g, 165 mmol) was added to a solution of 5-bromo-2-(6-chloropyridin-3-yloxy)-3-fluorobenzoic acid (38.2 g, 110 mmol) and diethylamine (63.3 mL, 606 mmol) in CH2Cl2 (500 mL) at 0° C. After stirring 5 hours at RT, the reaction was quenched with saturated aqueous sodium bicarbonate (250 mL) at RT and diluted with water (100 mL) and the organics was removed in vacuo. The mixture was diluted with EtOAc (250 mL) and the layers were separated and the aqueous layer was extracted with EtOAc (3×100 mL). The combined organic extracts were washed with saturated aqueous sodium bicarbonate, water, 1N HCl, water, brine, and dried over sodium sulfate. The solution was filtered and concentrated in vacuo to provide a residue that was purified by filtering through a pad of silica gel by eluting with 1:2 EtOAc in hexane to provide 5-bromo-2-(6-chloropyridin-3-yloxy)-N,N-diethyl-3-fluorobenzamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883782B2
Source datasetuspto-grants-2014_11
ORD IDord-6647e998ef0b4d86b54d9858f3f6337e
Source noteuspto-grants-2014_11