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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 714988Generated: November 3, 2026

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

https://huagongshe.com/reaction/714988

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 numberUS09187465B2
Source datasetuspto-grants-2015_11
ORD IDord-226a9e7bb439415ea52ea50fea74bc65
Source noteuspto-grants-2015_11