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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345646Generated: October 29, 2026

Water → 4-Chloromethyl-3-[2-(2-tritylamino-4-thiazolyl)-2-trityloxyimino-acetamido]-2-oxo-azetidine

https://huagongshe.com/reaction/345646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
Reactant4-Chloromethyl-3-amino-2-oxo-azetidine hydrochlorideHCID 19992113—
ReactantSodium 2-(2-tritylamino-4-thiazolyl)-2-trityloxyimino-acetic acidHCID 86743756—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
Product4-Chloromethyl-3-[2-(2-tritylamino-4-thiazolyl)-2-trityloxyimino-acetamido]-2-oxo-azetidineHCID 53647805—

Reaction Steps

A mixture of 1.527 g of the syn isomer of sodium 2-(2-tritylamino-4-thiazolyl)-2-trityloxyimino-acetic acid, 419 mg of tosyl chloride and 15 ml of methylene chloride was stirred for 40 minutes and then a solution of 342 mg of 4-chloromethyl-3-amino-2-oxo-azetidine hydrochloride in 15 ml of methylene chloride and 0.6 ml of triethylamine was added thereto. The mixture was stirred for 2 hours and water was added thereto with stirring. The decanted aqueous phase was extracted with methylene chloride and the combined organic phases were dried, filtered and evaporated to dryness under reduced pressure. The residue was chromatographed over silica gel and was eluted with ether to obtain 736 mg of syn isomer of 4-chloromethyl-3-[2-(2-tritylamino-4-thiazolyl)-2-trityloxyimino-acetamido]-2-oxo-azetidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05057512
Source datasetuspto-grants-1991_10
ORD IDord-8bc9b9e7bcff4201a5d63c1aea5eff1e
Source noteuspto-grants-1991_10