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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1513532Generated: November 4, 2026

4-Methylmorpholine → Z-Lys(Z)-Leu-Leu-OMe

https://huagongshe.com/reaction/1513532

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantN2,N6-Bis[(phenylmethoxy)carbonyl]-L-lysineHCID 7269422—
ReactantL-Leucine, L-leucyl-, methyl ester, hydrochloride (1:1)HCID 15598024—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductZ-Lys(Z)-Leu-Leu-OMeHCID 1202055199.7%

Reaction Conditions

Temperature19 °C

Reaction Steps

4-Methylmorpholine (1.26 g, 12.5 mmol) and HOBt (1.69 g, 12.5 mmol) were added to a solution of H-Leu-Leu-OMe.HCl (4.04 g, 13.75 mmol) in ethyl acetate (160.0 g) and DMF (36.0 g) over 15 min. Z-Lys(Z)—OH (5.18 g, 12.5 mmol) was added to this stirred mixture over 15 min. A solution of DCC (3.10 g, 12.5 mmol) in ethyl acetate (10.0 g) was added dropwise at 18-20° C. over 30 min. The reaction mixture was stirred at 18-20° C. for 16 h and filtered. The filter cake was washed with ethyl acetate (100.0 g) and the combined filtrate was washed with aqueous NaHCO3. The resulting organic layer was washed with aqueous NaCl and concentrated under reduced pressure. The residue was dissolved in MeOH (80.0 g) at about 50° C. Water (160 g) was slowly added and the mixture was stirred for about 1 h at 20° C. The resulting solid was filtered, washed with H2O (80.0 g) and dried at 40° C. in a vacuum oven to give 8.16 g, 99.6% of the product Z-Lys(Z)-Leu-Leu-OMe.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08217142B2
Source datasetuspto-grants-2012_07
ORD IDord-646b1901a08b45eb910cc851b5d4bd0d
Source noteuspto-grants-2012_07