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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249606Generated: October 29, 2026

4-Methylmorpholine → HCID 178525024, compound

https://huagongshe.com/reaction/249606

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 178525024HCID 178525024103.7%

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 numberUS05214037
Source datasetuspto-grants-1993_05
ORD IDord-9549b1e671324dd3b89ff9c3e48c8014
Source noteuspto-grants-1993_05