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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464215Generated: October 30, 2026

Methanol → Benzhydryl 7-amino-3-[2-(2-pyridyl)vinyl]-3-cephem-4-carboxylate

https://huagongshe.com/reaction/464215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPyridineHCID 1049—
ReactantPhosphorus pentachlorideHCID 24819—
ReactantBenzhydryl 7-phenylacetamido-3-[2-(2-pyridyl)vinyl]-3-cephem-4-carboxylateHCID 131714363—
SolventDichloromethaneHCID 6344—
ProductBenzhydryl 7-amino-3-[2-(2-pyridyl)vinyl]-3-cephem-4-carboxylateHCID 13171436468.8%

Reaction Steps

To a suspension of pyridine-phosphorus pentachloride complex prepared from pyridine (48 g) and phosphorus pentachloride (12.7 g) in methylene chloride (120 ml) was added benzhydryl 7-phenylacetamido-3-[2-(2-pyridyl)vinyl]-3-cephem-4-carboxylate (trans isomer) (12 g) under ice-cooling with stirring. The mixture was stirred at the same temperature for 30 minutes and poured into methanol (90 ml) at -25° C. The mixed solution was further stirred at -5° to -15° C. for 10 minutes and then was evaporated under reduced pressure. To the residue was added a mixture of tetrahydrofuran (200 ml), ethyl acetate (200 ml) and water (200 ml) and the mixture was adjusted to pH 6.5 with a saturated aqueous solution of sodium bicarbonate. The separated organic layer was washed with brine, dried over magnesium sulfate and evaporated to give benzhydryl 7-amino-3-[2-(2-pyridyl)vinyl]-3-cephem-4-carboxylate (trans isomer) (6.6 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04546101
Source datasetuspto-grants-1985_10
ORD IDord-c182730be7ac4f3d8b55e47dabf32b95
Source noteuspto-grants-1985_10