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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656186Generated: November 1, 2026

Pyridine → Benzhydryl 7-salicylideneamino-3-chloromethyl-3-cephem-4-carboxylate

https://huagongshe.com/reaction/1656186

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPhosphorus pentachlorideHCID 24819—
ReactantBenzhydryl 7-salicylideneamino-3-hydroxymethyl-3-cephem-4-carboxylateHCID 136460596—
SolventDichloromethaneHCID 6344—
ProductBenzhydryl 7-salicylideneamino-3-chloromethyl-3-cephem-4-carboxylateHCID 13646059985.9%

Reaction Conditions

Temperature-30 °C

Reaction Steps

Benzhydryl 7-salicylideneamino-3-hydroxymethyl-3-cephem-4-carboxylate (1.01 g) was dissolved in methylene chloride (10 ml) and cooled to -30° C. To this solution was added phosphorus pentachloride (0.46 g), followed by addition of pyridine (0.18 ml). The reaction mixture was stirred for an hour at -30° to -20° C. and poured into ice-water. The separated organic layer was washed with water and an aqueous sodium chloride, followed by drying over magnesium sulfate. The solvent was evaporated in vacuo to give benzhydryl 7-salicylideneamino-3-chloromethyl-3-cephem-4-carboxylate (0.9 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05252731
Source datasetuspto-grants-1993_10
ORD IDord-dd2ef802211940c0876a199863df7e43
Source noteuspto-grants-1993_10