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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249610Generated: October 27, 2026

Hydrochloric Acid → HCID 178525024, compound

https://huagongshe.com/reaction/249610

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-MethylmorpholineHCID 7972—
ReactantPhosphorodichloridic acid, phenyl esterHCID 13038—
Reactant2-(((1-(tert-Butoxy)-2-methyl-1-oxopropan-2-yl)oxy)imino)-2-(2-((tert-butoxycarbonyl)amino)thiazol-4-yl)acetic acidHCID 18963292—
ReactantHCID 178511753HCID 178511753—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 178525024HCID 178525024109.2%

Reaction Conditions

Temperature-30 °C

Reaction Steps

To a solution of 7β-amino-3-(trityl-1,2,3-triazol-4-ylthiomethylthio) -3-cephem-4-carboxylic acid diphenylmethyl ester (800 mg : 1.06 mMol.) and (Z)-2-(2-t-butoxycarbonylaminothiazol -4-yl)-2-(1 t-butoxycarbonyl-1methylethoxyimino)acetic acid (479 mg : 1.12 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 50 minutes. The reaction mixture is mixed 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 column chromatography (toluene : ethyl acetate=10:1 to 5:1) to give 7β-(Z)-2-(2-t-butoxycarbonylaminothiazol-4 yl)-2-(1-t-butoxycarbonyl -1-methylethoxyimino)acetamido]-3-(trityl-1,2,3-triazol-4-ylthiomethylthio) -3-cephem-4carboxylic acid diphenylmethyl ester (855 mg) as yellow foam. Yield : 69%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05214037
Source datasetuspto-grants-1993_05
ORD IDord-455523c480144033ad5ef1dd00e8f74a
Source noteuspto-grants-1993_05