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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349030Generated: October 25, 2026

Triethylamine → Methyl quinoline-7-carboxylate

https://huagongshe.com/reaction/349030

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantQuinolin-7-yl trifluoroacetateHCID 21087171—
ReactantN,N-dimethylformamide methanolHCID 21901440—
ProductMethyl quinoline-7-carboxylateHCID 12554532—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a stirred solution of quinolin-7-yl trifluoroacetate (750 mg, 2.7 mmol), PdCl2(Ph3P) (95 mg, 0.14 mmol), and triethylamine (1.2 mL, 8.4 mmol) in 1:2 DMF/MeOH (39 mL) was degassed and sparged with CO, and the mixture was heated at 60° C. for 48 h. The mixture was cooled to room temperature, filtered through diatomaceous earth, and concentrated under reduced pressure. The residue was diluted with a 5% solution of LiCl, and washed with CHCl3 (3×250 mL). The combined organics were dried (Na2SO4), filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica, 3:1 ethyl acetate/hexanes) provided methyl quinoline-7-carboxylate (185 mg): ESI MS m/z 188 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176242B2
Source datasetuspto-grants-2007_02
ORD IDord-9746052bf7c2496a99eb5d0e30515cb4
Source noteuspto-grants-2007_02