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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192507Generated: October 27, 2026

5-Chloro-7-{[methoxy(methyl)amino]carbonyl}quinolin-8-yl trifluoromethanesulfonate → 5-chloro-8-(3-fluorophenyl)-N-methoxy-N-methylquinoline-7-carboxamide

https://huagongshe.com/reaction/1192507

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-7-{[methoxy(methyl)amino]carbonyl}quinolin-8-yl trifluoromethanesulfonateHCID 86656172—
ReactantHCID 178505804HCID 178505804—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
Product5-chloro-8-(3-fluorophenyl)-N-methoxy-N-methylquinoline-7-carboxamideHCID 8665617989%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a mixture of 5-chloro-7-{[methoxy(methyl)amino]carbonyl}quinolin-8-yl trifluoromethanesulfonate (0.200 g, 0.502 mmol) in tetrahydrofuran (5 mL) was added 0.50 M (3-fluorophenyl)(iodo)zinc in tetrahydrofuran (1.20 mL, 0.602 mmol) with stirring, followed by addition of tetrakis(triphenylphosphine)palladium(0) (29.0 mg, 0.0251 mmol). The reaction mixture was heated at 60° C. overnight. After cooling to room temperature, the mixture was filtered and concentrated under reduced pressure. The crude mixture was purified on silica gel, eluting with 0 to 60% EtOAc in hexane, to give the desired product (154 mg, 89%). LCMS calculated for C18H15ClFN2O2(M+H)+: m/z=345.1; found: 345.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680108B2
Source datasetuspto-grants-2014_03
ORD IDord-13d2fa1fdd624155beec2810c72b9aaf
Source noteuspto-grants-2014_03