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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1782622Generated: October 30, 2026

Water → 4-Acetylamino-3-chloro-6-[2,4 dichloro-3-(1-fluoroethyl)phenyl]pyridine-2-carboxylic acid, methyl ester

https://huagongshe.com/reaction/1782622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCesium fluorideHCID 25953—
Reactant4-Acetylamino-3-chloro-6-trimethylstannylpyridine-2-carboxylic acid methyl esterHCID 22677308—
Reactant2,4 Dichloro-3-(1-fluoroethyl)-bromobenzeneHCID 68808916—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
Product4-Acetylamino-3-chloro-6-[2,4 dichloro-3-(1-fluoroethyl)phenyl]pyridine-2-carboxylic acid, methyl esterHCID 68808680—

Reaction Steps

A solution of 2,4 dichloro-3-(1-fluoroethyl)-bromobenzene (3.4 g, 12.5 mmol), 4-acetylamino-3-chloro-6-trimethylstannyl-pyridine-2-carboxylic acid, methyl ester (4.7 g, 12.5 mmol), copper iodide (0.4 g, 2.1 mmol), cesium fluoride (3.6 g, 25 mmol) and dichlorobis(triphenylphosphine)palladium (0.14 g, 2 mmol) in DMF (50 mL) was heated to 70° C. for 2 hours. Water (100 mL) was added the mixture extracted with ethyl acetate (2×100 mL). The combined extracts were washed with brine, dried (sodium sulfate) and concentrated. The residue was purified by chromatography (15%-30% ethyl acetate in hexanes) to give 4-acetylamino-3-chloro-6-[2,4 dichloro-3-(1-fluoroethyl)phenyl]pyridine-2-carboxylic acid, methyl ester which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07498468B2
Source datasetuspto-grants-2009_03
ORD IDord-b47ea4588ed34879940d3ad59339d2ce
Source noteuspto-grants-2009_03