Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 927441Generated: October 31, 2026

Pyridine → N~2~-(tert-Butoxycarbonyl)-L-leucinamide

https://huagongshe.com/reaction/927441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAmmonium HydroxideHCID 14923—
ReactantL-Leucine, N-((1,1-dimethylethoxy)carbonyl)-HCID 83170—
ReactantDi-tert-butyl dicarbonateHCID 90495—
SolventAcetonitrileHCID 6342—
ProductN~2~-(tert-Butoxycarbonyl)-L-leucinamideHCID 720129986%

Reaction Steps

A mixture of (S)-2-(tert-butoxycarbonylamino)-4-methylpentanoic acid (1.8 g), di-tert-butyl dicarbonate (CAN:24424-99-5, 12 mmol) and pyridine (3 mL) in CH3CN (50 mL) was stirred at room temperature for 20 min. Ammonium hydroxide solution (25%-28% NH3, 15 mL) was added dropwise during 30 min. The resulting reaction mixture was stirred overnight. During the removal of solvents, the product precipitated, was collected by filtration and dried to give the target compound as a white solid (1.55 g, 86%). MS (D): m/e=253.2 [M+Na]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290451B2
Source datasetuspto-grants-2016_03
ORD IDord-96d5367fa8bd4bf080b8db505e4aef3e
Source noteuspto-grants-2016_03