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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39758Generated: October 28, 2026

Trifluoroacetic acid → HCID 59397840, compound

https://huagongshe.com/reaction/39758

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 59398408HCID 59398408—
SolventChloroformHCID 6212—
ProductHCID 59397840HCID 59397840—

Reaction Steps

To 2 mL of a chloroform solution containing 280 mg of tert-butyl (1-(2-(7-methoxy-5-(pyridin-4-yl)-2-oxoquinoxalin-1(2H)-yl)ethyl)piperidin-4-yl)carbamate, 0.84 mL of trifluoroacetic acid was added, and the mixture was stirred at room temperature for 2 hours. The reaction mixture was concentrated under reduced pressure, chloroform and water were added thereto, the resultant solution was adjusted to pH about 12 with a 2 mol/L aqueous sodium hydroxide solution, and the organic layer was separated. The organic layer was washed with an aqueous saturated sodium chloride solution, and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure to obtain 230 mg of a yellow oily substance, 1-(2-(4-aminopiperidin-1-yl)ethyl)-7-methoxy-5-(pyridin-4-yl)quinoxalin-2(1H)-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524738B2
Source datasetuspto-grants-2013_09
ORD IDord-9ed6de9bd9584749bd9d96e119c22ebd
Source noteuspto-grants-2013_09