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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183484Generated: November 3, 2026

4-Methylmorpholine → N-benzyloxycarbonyl-L-leucyl-L-leucine t-butyl ester

https://huagongshe.com/reaction/2183484

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantLeucine, N-carboxy-, N-benzyl ester, L-HCID 74840—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactanttert-butyl (2S)-2-amino-4-methylpentanoate hydrochlorideHCID 12451443—
SolventDichloromethaneHCID 6344—
ProductN-benzyloxycarbonyl-L-leucyl-L-leucine t-butyl esterHCID 6000405099.5%

Reaction Steps

Under atmosphere of argon, to a solution of N-benzyloxycarbonylleucine (26.5 g) and leucine t-butyl ester hydrochloride (22.4 g) in methylene chloride (20.0 ml) were added 1-hydroxybenzotriazole (HOBt) (14.2 g) and 1-ethyl-3-[3-(dimethylamino)propyl]carbodiimide (EDC) hydrochloride (20.1 g) at 0° C. Thereto was added N-methylmorpholine (11.5 ml) over a period of 5 minutes and the mixture was stirred for 20 hours at room temperature. The reaction solution was concentrated and to the residue were added ice-water and ethyl acetate. In order to dissolve HOBt that appeared, was added sodium bicarbonate. The aqueous layer was extracted with ethyl acetate and combined organic layer was washed with 10% aqueous solution of citric acid, a saturated aqueous solution of sodium bicarbonate and saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate, and was concentrated to give the title compound (43.2 g) having the following physical data.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900207B2
Source datasetuspto-grants-2005_05
ORD IDord-56da08a448f5402580e05d6c7dc8a785
Source noteuspto-grants-2005_05