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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111755Generated: October 25, 2026

Dimethylformamide → 3-[(acetyloxy)methyl]-7-[[2-[4-(azidomethyl)phenyl]-acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid N-ethoxycarbonyl-N-methylaminoethyl ester

https://huagongshe.com/reaction/1111755

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodiumHCID 5360545—
ReactantEthyl N-(chloromethyl)-N-methylcarbamateHCID 15790124—
Reactant3-[(Acetyloxy)methyl]-7-[[2-[4-(azidomethyl)phenyl]acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acidHCID 22767758—
Product3-[(acetyloxy)methyl]-7-[[2-[4-(azidomethyl)phenyl]-acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid N-ethoxycarbonyl-N-methylaminoethyl esterHCID 54111057—

Reaction Steps

A mixture of 1.2 g of the sodium salt of 3-[(acetyloxy)-methyl]-7-[[2-[4-(azidomethyl]phenyl]acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid and 0.5 g of N-chloromethyl-N-methylurethane in 40 ml of dimethylformamide is stirred at room temperature for 2 hours. The mixture is poured into ice-water and decanted. The oily residue is taken up in 75 ml of ethyl acetate and washed with 5 ml of dilute aqueous sodium bicarbonate and 15 ml of water then dried over magnesium sulfate, filtered and evaporated to give 3-[(acetyloxy)methyl]-7-[[2-[4-(azidomethyl)phenyl]-acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid N-ethoxycarbonyl-N-methylaminoethyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04118562
Source datasetuspto-grants-1978_10
ORD IDord-c5a0c82c06f9442092166384c273c10b
Source noteuspto-grants-1978_10