Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2253988Generated: November 2, 2026

Hydrochloric Acid → HCID 178491514, compound

https://huagongshe.com/reaction/2253988

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyridineHCID 1049—
ReactantPhosphorus oxide (P4O10)HCID 14812—
Reactant4-Methoxybenzyl 7-amino-3-chloromethyl-3-cephem-4-carboxylateHCID 14032022—
Reactant(2Z)-2-(2-benzhydryloxy-2-oxo-1-thiophen-3-ylethoxy)imino-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetic acidHCID 19746691—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 178491514HCID 17849151493.4%

Reaction Conditions

Temperature-40 °C

Reaction Steps

(Z)-2-(2-tritylamino-4-thiazolyl)-2-[(diphenylmethyloxycarbonyl)(3-thienyl)methyl]oxyiminoacetic acid (1.90 g, 2.58 mmol) and phosphorus pentoxide (0.564 g, 2.71 mmol) were added to dichloromethane (11 ml) under ice-cooling, and then the resulting mixture was stirred for 30 min. Thus obtained solution was added at -60° C. to the solution of 4-methoxybenzyl 7-amino-3-chloromethyl-3-cephem-4-carboxylate (1.046 g, 2.58 mmol) and pyridine (1.04 ml, 12.9 mmol) in dichloromethane (30 ml) at -40° C. The reaction solution was allowed to -20° C. over 40 min. The reaction solution was cooled to -40° C., and 1N hydrochloric acid (12.9 ml) was added thereto. Water was added to the reaction solution, the solution was extracted with dichloromethane (×3), the organic layer was washed with a saturated saline and dried over anhydrous magnesium sulfate, and then the solvent was evaporated to give a caramel (3.50 g). The caramel was subjected to silica gel column chromatography eluting with hexane-ethyl acetate to obtain (4-methoxybenzyl) 7β-[(Z)-2-(2-tritylamino-4-thiazolyl)-2-[[(R S)-(diphenylmethyloxycarbonyl)(3-thienyl)methoxy]imino]acetamido]-3-cloromethyl-3-cephem-4-carboxylate (2.62 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05233035
Source datasetuspto-grants-1993_08
ORD IDord-84a519518a3147a9987183ba841ff8f0
Source noteuspto-grants-1993_08