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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 439745Generated: October 26, 2026

N-Methylpiperidine → N-(t-butoxycarbonyl)-L-valine 4-methoxy-1-phenylethylamide

https://huagongshe.com/reaction/439745

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylpiperidineHCID 12291—
ReactantIsobutyl chloroformateHCID 62365—
ReactantBoc-L-ValineHCID 83693—
Reactant1-(4-Methoxyphenyl)ethanamineHCID 238181—
SolventDichloromethaneHCID 6344—
ProductN-(t-butoxycarbonyl)-L-valine 4-methoxy-1-phenylethylamideHCID 14774435217.1%

Reaction Conditions

Temperature-60 °C

Reaction Steps

2.3 g (0.023 mol) of N-methylpiperidine are added to 5.0 g of t-butoxycarbonyl-L-valine (0.023 mol), dissolved in 50 ml of CH2Cl2, at -20° C. 3.2 g (0.023 mol) of isobutyl chloroformate are then rapidly added dropwise at -20° C., the mixture is subsequently stirred at the same temperature for 10 minutes and cooled to -60° C. and 3.5 g (0.023 mol) of 4-methoxy-1-phenylethylamine are allowed to run in, the temperature being kept below -15° C. After 2 hours at -15° C., the mixture is subsequently stirred at room temperature for 15 hours, the solid is filtered off and rinsed with CH2Cl2, the filtrate is concentrated, the residue is introduced into water, the mixture is extracted twice with ethyl acetate and the combined ethyl acetate phases are washed with NaHCO3 solution and water, dried and concentrated. 17.5 g (85% of theory) of N-(t-butoxycarbonyl)-L-valine 4-methoxy-1-phenylethylamide of melting point 126°-127° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05516786
Source datasetuspto-grants-1996_05
ORD IDord-836d11ad9b7c41dea4121f53b7b7fa49
Source noteuspto-grants-1996_05