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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2231512Generated: November 2, 2026

Phosphoric Acid → Sodium 3-[2-(2-chloroacetamido-4-thiazolyl)-2-methoxyiminoacetamido]-3-methoxy-2-oxoazetidine-1-sulfonate

https://huagongshe.com/reaction/2231512

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphoric AcidHCID 1004—
ReactantSodium BicarbonateHCID 516892—
ReactantC8H8ClN3O4SHCID 581157—
Reactant3-Amino-3-methoxy-2-oxoazetidine-1-sulfonic acidHCID 13019097—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductSodium 3-[2-(2-chloroacetamido-4-thiazolyl)-2-methoxyiminoacetamido]-3-methoxy-2-oxoazetidine-1-sulfonateHCID 86741497—

Reaction Steps

In 1 ml of water is dissolved 30 mg of the above 3-amino-3-methoxy-2-oxoazetidine-1-sulfonic acid, and to the solution are added a solution of 89 mg of the acid chloride prepared from 2-(2-chloroacetamido-4-thiazolyl)-2-methoxyiminoacetic acid (syn-isomer) in 1 ml of tetrahydrofuran and 36 mg of sodium hydrogen carbonate in alternate portions with ice-cooling and stirring. The mixture is further stirred at room temperature for 20 minutes and adjusted to pH 5.8 with phosphoric acid. After removal of tetrahydrofuran under reduced pressure, the water layer is washed with ethyl acetate and purified by Amberlite XAD-II chromatography. The above procedure yields 28 mg of sodium 3-[2-(2-chloroacetamido-4-thiazolyl)-2-methoxyiminoacetamido]-3-methoxy-2-oxoazetidine-1-sulfonate (syn-isomer) which is the same compound as the one described in Example 9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04782147
Source datasetuspto-grants-1988_11
ORD IDord-31c14b3fbfab46d8b97c48cf9f094a12
Source noteuspto-grants-1988_11