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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383821Generated: October 26, 2026

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

https://huagongshe.com/reaction/383821

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 numberUS08367676B2
Source datasetuspto-grants-2013_02
ORD IDord-b580b5d4272f4463836fc647cd6041a1
Source noteuspto-grants-2013_02