Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264974Generated: October 25, 2026

4-Methylmorpholine → (S)-N-(2-Phthalimido-1-oxohexyl)glycine, ethyl ester

https://huagongshe.com/reaction/264974

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantGlycine ethyl ester, hydrochlorideHCID 2723640—
Reactant(S)-2-Phthalimido-6-hydroxyhexanoic acidHCID 11065730—
ReactantHCID 178418300HCID 178418300—
SolventDimethylformamideHCID 6228—
Product(S)-N-(2-Phthalimido-1-oxohexyl)glycine, ethyl esterHCID 131719537—

Reaction Steps

A slurry of glycine, ethyl ester, hydrochloride salt (2.718 g, 19.5 mmol.) in dimethylformamide (36 ml.) was treated with 4-methyl morpholine (2.60 ml., 2.39 g., 23.6 mmol.) and stirred at room temperature for 5 minutes. The mixture was then treated with (S)-2-phthalimido-6-hydroxyhexanoic acid (4.50 g., 16.2 mmol.) and hydroxybenzotriazole (2.225 g., 16.5 mmol.), cooled to 0° C., and then treated with ethyl-3-(3-dimethylamino)propyl carbodiimide, hydrochloride salt (3.438 g., 17.9 mmol.). After stirring at 0° C. for 1 hour and at room temperature for 2 hours, the mixture was partitioned between ethyl acetate and 0.5N hydrochloric acid and subsequently extracted three times with ethyl acetate. The pooled ethyl acetate extracts were washed in succession with water, saturated sodium bicarbonate, and brine, then dried (sodium sulfate), filtered and stripped to give 5.77 g. of title product as a colorless oil. TLC (ethyl acetate) Rf =0.34.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05646276
Source datasetuspto-grants-1997_07
ORD IDord-c6bea37cfe6e4c79b34e6c6da2b88737
Source noteuspto-grants-1997_07