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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1267569Generated: November 1, 2026

Ethylmorpholine → N-(cyclohexylglycyl-glutaminyl-serinyl)leucine benzyl ester hydrochloride

https://huagongshe.com/reaction/1267569

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylmorpholineHCID 7525—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
ReactantN-(glutaminyl-serinyl)leucine benzyl ester hydrochlorideHCID 69996228—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductN-(cyclohexylglycyl-glutaminyl-serinyl)leucine benzyl ester hydrochlorideHCID 69994356—

Reaction Conditions

Temperature20 °C

Reaction Steps

N-(glutaminyl-serinyl)leucine benzyl ester hydrochloride (2.6 kg) (prepared as described in Step 3), N-Boc-L-cyclohexylglycine (1.414 kg) and HOBt hydrate (168 g) were dissolved in DMF (13.0 L). N-ethylmorpholine (1.266 kg, 11.0 M) and EDC hydrochloride (1.265 kg) were added and the mixture stirred at 20° C. for 3 hours. The solution was diluted with ethyl acetate (13.0 L) and water (26.0 L) added. The product precipitated and the slurry was stirred at room temperature for 1 hour. The solid was collected by filtration, washed with 1:1 ethyl acetate/water (60 L) dried on the filter under nitrogen for 24 hours and dried in vacuo at 45°. The title compound was obtained as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06552166B1
Source datasetuspto-grants-2003_04
ORD IDord-b47cdf6dce524e43b881edd3d3fc367c
Source noteuspto-grants-2003_04