Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2231564Generated: November 1, 2026

Water → cis-4-Acetoxymethyl-3-[2-(2-chloroacetamido-4-thiazolyl)-2-methoxyiminoacetamido]-2-oxoazetidine

https://huagongshe.com/reaction/2231564

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium BicarbonateHCID 516892—
Reactant2-(2-Chloroacetamido-4-thiazolyl)-2-methoxyiminoacetyl chlorideHCID 53800150—
Reactantcis-4-Acetoxymethyl-3-amino-2-oxoazetidineHCID 70390316—
SolventTetrahydrofuranHCID 8028—
Productcis-4-Acetoxymethyl-3-[2-(2-chloroacetamido-4-thiazolyl)-2-methoxyiminoacetamido]-2-oxoazetidineHCID 86740461—

Reaction Steps

Under ice-cooling and stirring, 12 ml of an aqueous solution containing 632 mg of cis-4-acetoxymethyl-3-amino-2-oxoazetidine and 1.122 g of sodium hydrogen carbonate is added to a suspension of 2.36 of 2-(2-chloroacetamido-4-thiazolyl)-2-methoxyiminoacetyl chloride (syn-isomer) in 20 ml of tetrahydrofuran. The mixture is stirred for 2 hours at room temperature and the solvent is then distilled off in vacuo to leave the residue, which solidifies. Water is added to the solidified residue, followed by filtration. The collected crystals are washed successively with an aqueous sodium hydrogen carbonate solution, water and ether and dried to give cis-4-acetoxymethyl-3-[2-(2-chloroacetamido-4-thiazolyl)-2-methoxyiminoacetamido]-2-oxoazetidine (syn-isomer), m.p. 180°-190° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04782147
Source datasetuspto-grants-1988_11
ORD IDord-19c0ace6bf31437eb4c7260f3466f237
Source noteuspto-grants-1988_11