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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1199584Generated: November 4, 2026

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

https://huagongshe.com/reaction/1199584

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—
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 triethylaime 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 numberUS04900728
Source datasetuspto-grants-1990_02
ORD IDord-f1478550fd764cb493ecbe303e62133e
Source noteuspto-grants-1990_02