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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2211191Generated: October 25, 2026

Pyridine → Nalpha-Cinnamoyl-L-lysine

https://huagongshe.com/reaction/2211191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant3-Phenylprop-2-enoyl chlorideHCID 66023—
Reactant(2S)-2-amino-6-(((tert-butoxy)carbonyl)amino)hexanoic acidHCID 2733283—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
ProductNalpha-Cinnamoyl-L-lysineHCID 53746252—

Reaction Steps

Nε-t-Butoxycarbonyl-L-lysine (2.58 g) was dissolved in 50 ml of dimethylformamide, and 30 ml of anhydrous pyridine was added to the solution. To the mixture was added a solution of cinnamoyl chloride in chloroform (1.665 g/20 ml) was added, and the reaction was carried out at 40° C. The reaction mixture was concentrated to dryness under reduced pressure, the residue was dissolved in 3.6N HCl/dioxane (33 ml) and, after 4 hours of standing, the solution was concentrated under reduced pressure to give the desired compound (2.43 g; hereinafter referred to as compound B).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05462976
Source datasetuspto-grants-1995_10
ORD IDord-4e16ae6f99d942be8a3aaed7f4c08f98
Source noteuspto-grants-1995_10