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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 240852Generated: October 30, 2026

Trifluoroacetic acid → HCID 50991728, compound

https://huagongshe.com/reaction/240852

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 50991642HCID 50991642—
SolventDichloromethaneHCID 6344—
ProductHCID 50991728HCID 50991728—

Reaction Steps

Trifluoroacetic acid (0.2 mL) was added to a mixture solution of tert-butyl 4-(3-(4-(2-(dimethylamino)ethoxy)phenyl)-1-(pyridin-4-yl)-1H-indol-6-yl)piperazine-1-carboxylate (4.1 mg, 7.6 μmol) in methylene chloride (0.2 mL) at room temperature. After stirring for 15 hours, the reaction solution was concentrated under reduced pressure. After adding ethyl acetate and saturated sodium bicarbonate aqueous solution, the mixture was extracted with ethyl acetate. The collected organic layer was washed with brine and concentrated under reduced pressure by drying with anhydrous magnesium sulfate. The target compound was obtained as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08648089B2
Source datasetuspto-grants-2014_02
ORD IDord-09b5b9bb12324e97b20a4ed64b2365c7
Source noteuspto-grants-2014_02