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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1431773Generated: November 2, 2026

Trifluoroacetic acid → HCID 59631180, compound

https://huagongshe.com/reaction/1431773

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 59631067HCID 59631067—
SolventDichloromethaneHCID 6344—
ProductHCID 59631180HCID 59631180—

Reaction Steps

A solution of 7-fluoro-N-(4-methoxybenzyl)-3-methyl-2-(pyridin-2-yl)quinolin-4-amine (0.900 g, 2.410 mmol), trifluoroacetic acid (2.8 mL, 36.2 mmol), and DCM (4 mL) was stirred at 23° C. for 1 hour. Upon completion, the reaction was concd, and the resulting residue was partitioned between EtOAc and 1 N HCl. The aqueous layer was then basified, and the product extracted twice with EtOAc. The combined organics were dried over magnesium sulfate and concd, affording 7-fluoro-3-methyl-2-(pyridin-2-yl)quinolin-4-amine as a beige amorphous solid. Mass Spectrum (ESI) m/e=254.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940724B2
Source datasetuspto-grants-2015_01
ORD IDord-10ae03fa55f94c9cb27cbf806449fa05
Source noteuspto-grants-2015_01