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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23565Generated: October 29, 2026

Trifluoroacetic acid → 4-Amino-1-(5-piperid-1-ylcarbonyl-2-pyridyl)piperidine

https://huagongshe.com/reaction/23565

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant4-Tert-butoxycarbonylamino-1-(5-piperid-1-ylcarbonyl-2-pyridyl)piperidineHCID 22574453—
SolventDichloromethaneHCID 6344—
Product4-Amino-1-(5-piperid-1-ylcarbonyl-2-pyridyl)piperidineHCID 11300700—

Reaction Steps

A solution of 0.475 g of 4-tert-butoxycarbonylamino-1-(5-piperid-1-ylcarbonyl-2-pyridyl)piperidine (1.24 mmol) and 5 ml of trifluoroacetic acid in 20 ml of dichloromethane is stirred for 1 hour. The reaction medium is concentrated under reduced pressure and then taken up in dichloromethane. The solution is basified (pH=9) using saturated aqueous sodium carbonate solution. The aqueous phase is extracted five times with dichloromethane. The organic phases are dried over magnesium sulfate and concentrated under reduced ressure. The 4-amino-1-(5-piperid-1-ylcarbonyl-2-pyridyl)piperidine is obtained in the form of an oil (0.310 g, 88%). [M+H+]=289.4

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06852736B2
Source datasetuspto-grants-2005_02
ORD IDord-a2f089456b464a99be748955170ba9f6
Source noteuspto-grants-2005_02