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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 890926Generated: October 27, 2026

4-Methylmorpholine → N-(benzylsulfonyl)-D-isoleucyl-L-methionine methyl ester

https://huagongshe.com/reaction/890926

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantL-Methionine, methyl ester, hydrochlorideHCID 11435579—
ReactantN-(benzylsulfonyl)-D-isoleucineHCID 36688801—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductN-(benzylsulfonyl)-D-isoleucyl-L-methionine methyl esterHCID 6962370567.1%

Reaction Steps

To a solution of N-(benzylsulfonyl)-D-isoleucine (6.3 g, 22.2 mmol) and L-methionine methyl ester hydrochloride (6.7 g, 33.3 mmol) in dichloromethane (100 ml), HOBt (4.1 g, 26.6 mmol), EDC HCl (5.1 g, 1.2 mmol) and N-methylmorpholine (3.4 g, 33.3 mmol) were added and stirred at room temperature under a nitrogen stream. After 12 hours, water was added to the reaction mixture, which was then extracted with ethyl acetate. The ethyl acetate layer was washed sequentially with 10% aqueous citric acid, saturated aqueous sodium bicarbonate and saturated brine, and then dried over anhydrous magnesium sulfate. After magnesium sulfate was filtered off, the filtrate was concentrated under reduced pressure and the residue was applied to flash column chromatography (Merck Silicagel 60; mobile phase: dichloromethane) to give N-(benzylsulfonyl)-D-isoleucyl-L-methionine methyl ester (6.4 g, 14.9 mmol; yield 67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07001887B2
Source datasetuspto-grants-2006_02
ORD IDord-9b33fd25ae764fea9b46b84287d2df49
Source noteuspto-grants-2006_02