Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1900206Generated: October 30, 2026

N-Methylpiperidine → N-isopropoxycarbonyl-L-valyl-N-(4-cyanophenyl)glycinamide

https://huagongshe.com/reaction/1900206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylpiperidineHCID 12291—
ReactantIsobutyl chloroformateHCID 62365—
Reactant(2S)-3-methyl-2-(((propan-2-yloxy)carbonyl)amino)butanoic acidHCID 11063514—
Reactant2-amino-N-(4-cyanophenyl)acetamideHCID 18788946—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductN-isopropoxycarbonyl-L-valyl-N-(4-cyanophenyl)glycinamideHCID 6763878548.6%

Reaction Conditions

Temperature-20 °C

Reaction Steps

0.3 g of N-methylpiperidine was added to a solution containing 0.6 g of N-isopropoxycarbonyl-L-valine dissolved in 40 ml of methylene chloride, at -20° C. After the mixture was stirred for 10 minutes at the same temperature, 0.4 g of isobutyl chloroformate was added to the n-fixture, and stirred for 1 hour at -20° C. 0.5 g of N1 -(4-cyanophenyl)glycinamide was added to this mixture at -60° C., and then the reaction mixture was allowed to sit and warm naturally to room temperature while being stirred, and was stirred for 20 hours at room temperature. Water was subsequently added to the reaction mixture. After the methylene chloride layer was washed successively with a 5% aqueous solution of sodium bicarbonate and water, the organic layer was dried over anhydrous magnesium sulfate and the methylene chloride was removed under reduced pressure. The residue was purified by column chromatography on silica gel, thus obtaining 0.5 g of the desired product in the form of colorless powder (yield: 49%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05574064
Source datasetuspto-grants-1996_11
ORD IDord-c0c2d90151594b849f00f86a58919815
Source noteuspto-grants-1996_11