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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 533402Generated: October 25, 2026

3,5-Difluoropyridine → Methyl 4-chloro-1-(3,5-difluoropyridin-4-yl)isoquinoline-7-carboxylate

https://huagongshe.com/reaction/533402

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-DifluoropyridineHCID 642820—
ReactantMethyl 4-chloro-1-{[(trifluoromethyl)sulfonyl]oxy}isoquinoline-7-carboxylateHCID 86666251—
ReactantButyllithiumHCID 178418339—
CatalystZincchlorideHCID 3007855—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 4-chloro-1-(3,5-difluoropyridin-4-yl)isoquinoline-7-carboxylateHCID 6777447220.8%

Reaction Steps

Under argon gas atmosphere, n-butyllithium (1.6 M THF solution, 0.7 mL) was added dropwise to a mixture of 3,5-difluoropyridine (123 mg) and THF (3 mL) at −78° C., followed by stirring at the same temperature for one hour. Then, zinc chloride (146 mg) was added, and stirred for an additional hour. Methyl 4-chloro-1-{[(trifluoromethyl)sulfonyl]oxy}isoquinoline-7-carboxylate (330 mg) and tetrakis(triphenylphosphine)palladium (206 mg) were added thereto, followed by heating under stirring in an oil bath at 60° C. for 3 hours. The reaction mixture was concentrated under reduced pressure and purified under silica gel column chromatography (hexane/ethyl acetate) to obtain methyl 4-chloro-1-(3,5-difluoropyridin-4-yl)isoquinoline-7-carboxylate (62 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853242B2
Source datasetuspto-grants-2014_10
ORD IDord-684a031afcaa4e1b8a4c20dd142e9d36
Source noteuspto-grants-2014_10