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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733664Generated: October 25, 2026

4-Methylmorpholine → Ethyl N-(1-((benzyloxy)carbonyl)-L-prolyl)-L-leucinate

https://huagongshe.com/reaction/1733664

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantBenzyloxycarbonyl-L-prolineHCID 101987—
ReactantL-Leucine, ethyl ester, hydrochloride (1:1)HCID 11658447—
Reactant4-Oxo-3,4-dihydro-3-methanesulfonyloxy-1,2,3-benzotriazineHCID 21896281—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
SolventEthyl AcetateHCID 8857—
ProductEthyl N-(1-((benzyloxy)carbonyl)-L-prolyl)-L-leucinateHCID 645307566.4%

Reaction Steps

N-Benzyloxycarbonyl-L-proline (1.25 g), L-leucine ethyl ester hydrochloride (1.00 g) and N-methylmorpholine (1.10 ml) are dissolved in chloroform (10 ml) and thereto is added 4-oxo-3,4-dihydro-3-methanesulfonyloxy-1,2,3-benzotriazine (1.20 g). After allowing to stand overnight, to the mixture are added water and ethyl acetate. The ethyl acetate layer is washed and dried, and then the solvent is distilled off to give N-(N-benzyloxycarbonyl-L-prolyl)-L-leucine ethyl ester (1.3 g), melting point: 65°-67° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04242507
Source datasetuspto-grants-1980_12
ORD IDord-89cf0924f3e74005978288a0de1fd424
Source noteuspto-grants-1980_12