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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707458Generated: October 30, 2026

4-Methylmorpholine → HCID 178452982, compound

https://huagongshe.com/reaction/1707458

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantPhosphorodichloridic acid, phenyl esterHCID 13038—
Reactant2-(2-((tert-Butoxycarbonyl)amino)thiazol-4-yl)acetic acidHCID 15480006—
ReactantHCID 178511753HCID 178511753—
SolventDichloromethaneHCID 6344—
ProductHCID 178452982HCID 17845298277%

Reaction Conditions

Temperature-30 °C

Reaction Steps

To a solution of 7β-amino-3-(trityl-1,2,3-triazol-4-ylthiomethyl-thio)-3-cephem-4-carboxylic acid diphenylmethyl ester (800 mg: 1.06 mMol.) and 2-(2-t-butoxycarbonylaminothiazol-4-yl)acetic acid (287 mg: 1.11 mMol.) in dichloromethane (8 ml) cooling at -30° C. are added N-methylmorpholine (0.27 ml: 2.46 mMol.) and phenyl dichlorophosphate (0.19 ml: 1.27 mMol.), and the mixture is stirred at -30° C. for 40 minutes. The reaction mixture is quenched with 10% hydrochloric acid (1 ml), diluted with water, and extracted with ethyl acetate. The extract is washed with brine, dried over sodium sulfate, and concentrated. The residue is purified by silica gel chromatography (toluene: ethyl acetate=3:1) to give 7β-[2-(2-t-butoxycarbonylaminothiazol-4-yl)acetamido]-3-(trityl-1,2,3-triazol-4-ylthiomethylthio)-3-cephem-4-carboxylic acid diphenylmethyl ester (812 mg) as pale yellow foam. Yield: 77%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05352792
Source datasetuspto-grants-1994_10
ORD IDord-f0cca37eb1d7422594e67a5d6903a4bb
Source noteuspto-grants-1994_10