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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706530Generated: October 30, 2026

4-Methylmorpholine → 1-(1-Methoxycarbonyl-2-methylpropyl)-3-(2-phenylacetamido)-2-azetidinone

https://huagongshe.com/reaction/1706530

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant1-(p-Chlorobenzenesulfonyloxy)-6-chloro-1,2,3-benzotriazoleHCID 12222841—
Reactant3-(1-Methoxycarbonyl-2-methylpropylamino)-2-(2-phenylacetamido)propionic acidHCID 54392562—
SolventEthyl AcetateHCID 8857—
Product1-(1-Methoxycarbonyl-2-methylpropyl)-3-(2-phenylacetamido)-2-azetidinoneHCID 539575461.1%

Reaction Steps

3-(1-Methoxycarbonyl-2-methylpropylamino)-2-(2-phenylacetamido)propionic acid (0.92 g) was dissolved in ethyl acetate (100 ml), and to the solution, there were added 4-methylmorpholine (0.66 g) and 1-(4-chlorobenzenesulfonyloxy)-6-chloro-1H-benzotriazole (1.11 g) under ice-cooling. The mixture was stirred at the same temperature for 18 hours and the insoluble materials were removed by filtration from the reaction mixture and ice-water (30 ml) was poured into the filtrate, whereafter the resultant mixture was stirred enough. The ethyl acetate layer was separated from the mixture, washed three times with an aqueous sodium bicarbonate and once with water, and then dried over magnesium sulfate. The solution was evaporated to dryness under reduced pressure to give a residue, which was subjected to column chromatography on silica gel (15 g). Elution was carried out with chloroform and the fractions containing a desired compound were collected. The solvent was removed by distillation from the eluate under reduced pressure to give 1-(1-methoxycarbonyl-2-methylpropyl)-3-(2-phenylacetamido)-2-azetidinone (10 mg), mp 105° to 107° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04207234
Source datasetuspto-grants-1980_06
ORD IDord-3efb43a21f2b43958bb36e412daaadf5
Source noteuspto-grants-1980_06