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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 240848Generated: October 30, 2026

Trifluoroacetic acid → HCID 50991638, compound

https://huagongshe.com/reaction/240848

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 50991548HCID 50991548—
SolventDichloromethaneHCID 6344—
ProductHCID 50991638HCID 5099163864%

Reaction Steps

Trifluoroacetic acid (46 μL, 0.059 mmol) was added to a mixture solution of tert-butyl 4-(3-(4-methoxyphenyl)-1-(pyridin-4-yl)-1H-indol-6-yl)piperazine-1-carboxylate (29 mg, 0.059 mmol) in methylene chloride (1 mL) at room temperature. After stirring for 3 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 (14 mg, 64%) was obtained as yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08648089B2
Source datasetuspto-grants-2014_02
ORD IDord-078dc0f7d654424d8350128f0b197f62
Source noteuspto-grants-2014_02