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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892691Generated: October 27, 2026

4-Methylmorpholine → benzyloxycarbonyl-L-histidyl-glycine amide

https://huagongshe.com/reaction/892691

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantIsobutyl chloroformateHCID 62365—
ReactantGlycinamide hydrochlorideHCID 2723639—
ReactantHCID 178523877HCID 178523877—
SolventTetrahydrofuranHCID 8028—
Productbenzyloxycarbonyl-L-histidyl-glycine amideHCID 178514040—

Reaction Steps

Na -t-butyloxycarbonyl-Nim -benzyloxycarbonyl-L-histidine was dissolved in tetrahydrofuran (THF) and neutralized with one equivalent of N-methylmorpholine. It was then coupled with glycinamide hydrochloride using isobutyl chloroformate and N-methylmorpholine. After two hours at -20° C. and an additional hour at ambient temperature, the reaction was quenched with 2N aqueous potassium bicarbonate. This product was extracted into ethyl acetate, washed with 1M aqueous citric acid, and saturated sodium bicarbonate. The organic phase was dried over anhydrous sodium sulfate. Filtration and evaporation gave Na -t-butyloxycarbonyl-Nim -benzyloxycarbonyl-L-histidyl-glycine amide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05118665
Source datasetuspto-grants-1992_06
ORD IDord-d3d0f0ba26784da8bc79687d4d6c20f0
Source noteuspto-grants-1992_06