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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192257Generated: October 30, 2026

Trifluoroacetic acid → HCID 50991638, compound

https://huagongshe.com/reaction/2192257

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 numberUS08329708B2
Source datasetuspto-grants-2012_12
ORD IDord-a5d5ef68256347cdaecbaea523361708
Source noteuspto-grants-2012_12