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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1860423Generated: October 31, 2026

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

https://huagongshe.com/reaction/1860423

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 numberUS06531471B2
Source datasetuspto-grants-2003_03
ORD IDord-3f69b16320744df4a7169b5d921874a5
Source noteuspto-grants-2003_03