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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 133010Generated: October 27, 2026

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

https://huagongshe.com/reaction/133010

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 numberUS07390804B2
Source datasetuspto-grants-2008_06
ORD IDord-cbd0bdc1d1a141ffb0f68f051d9fe1fa
Source noteuspto-grants-2008_06