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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278923Generated: October 27, 2026

Tert-butoxycarbonylalanine → N-(tert-Butoxycarbonyl)-L-alanine 4-(2-pyridyl)piperidin-1-yl amide

https://huagongshe.com/reaction/278923

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butoxycarbonylalanineHCID 85082—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant2-(Piperidin-4-yl)pyridineHCID 10374750—
SolventDichloromethaneHCID 6344—
ProductN-(tert-Butoxycarbonyl)-L-alanine 4-(2-pyridyl)piperidin-1-yl amideHCID 18712694107.1%

Reaction Steps

To a solution of N-(tert-butoxycarbonyl)-L-alanine (1.485 g, 7.847 mmol) and 4-(2-pyridyl)piperidine (0.910 g, 5.60 mmol) in dichloromethane (20 mL) at 0° C., was added N,N-dimethylaminopyridine (DMAP, 2.05 g, 16.8 mmol) and 1-(3-dimethylaminopropyl)3-ethylcarbodiimide hydrochloride (DMAPECD, 2.147 g, 11.2 mmol). The resulting mixture was stirred overnight while warmed up to room temperature. The reaction mixture was quenched with aqueous NH4Cl (30 mL) and extracted with CH2Cl2 (30 mL×2). The combined extracts were dried (K2CO3). concentrated, and purified by flash chromatography on silica gel (100% EtOAc) to obtain 2.09 g (80%) of N-(tert-Butoxycarbonyl)-L-alanine 4-(2-pyridyl)piperidin-1-yl amide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06362182B1
Source datasetuspto-grants-2002_03
ORD IDord-d1f78311d59148578cd12b2b3e7679c5
Source noteuspto-grants-2002_03