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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389756Generated: October 30, 2026

4-Aminobenzoic Acid → Tert-butyl 4-((4-aminobenzamido)methyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/389756

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Aminobenzoic AcidHCID 978—
Reactant4-MethylmorpholineHCID 7972—
Reactant1-Boc-4-(aminomethyl)piperidineHCID 736817—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 4-((4-aminobenzamido)methyl)piperidine-1-carboxylateHCID 59587665—

Reaction Steps

To a solution of 4-(aminomethyl)-Boc-piperidine (0.313 g, 1.458 mmol), 4-aminobenzoic acid (0.200 g, 1.458 mmol) and N-methyl morpholine (0.242 mL, 2.187 mmol) in dichloromethane (2 mL) was added 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (0.422 g, 2.187 mmol) and the reaction mixture stirred at room temperature overnight. The reaction was then washed with water and brine. The organic phase was dried over MgSO4 and the solvent removed in vacuo. The residue was purified by silica gel column chromatography using a 0-100% EtOAc in hexane gradient to afford tert-butyl 4-((4-aminobenzamido)methyl)piperidine-1-carboxylate. LCMS (3) Rt: 1.91 min; m/z (ES+) 334.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08378095B2
Source datasetuspto-grants-2013_02
ORD IDord-64b941160c134fe59b7346da36d702fc
Source noteuspto-grants-2013_02