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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807720Generated: October 26, 2026

Trifluoroacetic acid → (4-Amino-3-fluorophenyl)(piperazin-1-yl)methanone

https://huagongshe.com/reaction/1807720

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl 4-(4-amino-3-fluorobenzoyl)piperazine-1-carboxylateHCID 58055815—
SolventDichloromethaneHCID 6344—
Product(4-Amino-3-fluorophenyl)(piperazin-1-yl)methanoneHCID 63187976—

Reaction Steps

tert-Butyl 4-(4-amino-3-fluorobenzoyl)piperazine-1-carboxylate (0.649 mmol, 210 mg) was stirred with dichloromethane (˜2 mL) and trifluoroacetic acid (˜0.5 mL) overnight. The mixture was purified by SCX chromatography to give the intermediate (4-amino-3-fluorophenyl)(piperazin-1-yl)methanone. 2-(4-(Bromomethyl)phenyl)-1,1,1,3,3,3-hexafluoropropan-2-ol (0.649 mmol, 219 mg), potassium carbonate (0.649 mmol, 90 mg) and acetonitrile (5 mL) were added to the intermediate (4-amino-3-fluorophenyl)(piperazin-1-yl)methanone and the mixture was stirred for 6 hours. The reaction mixture was concentrated under reduced pressure. The residue obtained was stirred in dichloromethane, filtered and the filtrate was purified by silica chromatography (eluting with dichloromethane increasing to ethyl acetate) to afford the title compound (46 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357679B2
Source datasetuspto-grants-2013_01
ORD IDord-1a4b70f9c88d4e0d85cd87c1c02093c0
Source noteuspto-grants-2013_01