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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535649Generated: October 27, 2026

Trifluoroacetic acid → 1-(5-(2-(Piperazin-1-yl)ethyl)indolin-1-yl)ethanone

https://huagongshe.com/reaction/535649

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl 4-(2-(1-acetylindolin-5-yl)ethyl)piperazine-1-carboxylateHCID 59636762—
SolventDichloromethaneHCID 6344—
Product1-(5-(2-(Piperazin-1-yl)ethyl)indolin-1-yl)ethanoneHCID 59636747101.8%

Reaction Steps

Trifluoroacetic acid (4.08 mL, 53.08 mmol) was added to a solution of tert-butyl 4-(2-(1-acetylindolin-5-yl)ethyl)piperazine-1-carboxylate (0.793 g, 2.12 mmol) in dry DCM and the reaction was stirred at room temperature for 60 min. The mixture was evaporated and the crude mixture was made basic with 10% NaOH aq. The aq phase was extracted with DCM (3×), dried (Na2SO4), filtered and evaporated to give 0.590 g of the product. This product was taken to the next step assuming quantitative yield without further purification. MS (ES+) m/z 274.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859534B2
Source datasetuspto-grants-2014_10
ORD IDord-385d2204b28b418eb06835bd6ce6981d
Source noteuspto-grants-2014_10