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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497115Generated: October 31, 2026

Trifluoroacetic acid → HCID 71556553, compound

https://huagongshe.com/reaction/1497115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 86682966HCID 86682966—
SolventDichloromethaneHCID 6344—
ProductHCID 71556553HCID 7155655374%

Reaction Steps

A solution of tert-butyl 6-chloro-2-(isopropyl(methyl)amino)-4-phenylquinoline-3-carboxylate (75 mg, 183 μmol), in DCM (1 ml) and TFA (1 ml) was stirred at room temperature for 2 h followed by a further 2 h at 40° C. The reaction mixture was concentrated in vacuo and the crude residue was dissolved in ethyl actetate and washed with water. The ethyl acetate layer was washed with 0.1N NaOH solution (2×) and then the aqueous layer was made acidic (pH 3-4) with 1N HCl and then further extracted with ethyl acetate. The organic layers were combined, dried over Na2SO4, filtered and concentrated in vacuo to give the desired product as a light yellow solid (48 mg, 74%). MS (ESI): 355 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199938B2
Source datasetuspto-grants-2015_12
ORD IDord-1d0437f72d7f4f899a49bc018d9636fe
Source noteuspto-grants-2015_12