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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1462739Generated: October 29, 2026

Methanol → p-Nitrobenzyl 7-amino-3-cephem-4-carboxylate

https://huagongshe.com/reaction/1462739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPyridineHCID 1049—
ReactantPhosphorus pentachlorideHCID 24819—
Reactantp-Nitrobenzyl 7-phenylacetamido-3-cephem-4-carboxylateHCID 70362156—
SolventDichloromethaneHCID 6344—
Productp-Nitrobenzyl 7-amino-3-cephem-4-carboxylateHCID 12775080101.7%

Reaction Conditions

Temperature10 °C

Reaction Steps

To a suspension of p-nitrobenzyl 7-phenylacetamido-3-cephem-4-carboxylate (10.50 g.) in dry dichloromethane (100 ml.) was added dry pyridine (2.14 g.). Phosphorus pentachloride (5.50 g.) was added to the solution at -10° C., and the mixture was stirred at -5° C. for 45 minutes and further at 10° C. for an hour. After adding methanol (520 g.) to the resultant mixture, the mixture was stirred at -20° C. for 1.5 hours. The precipitates were collected by filtration, washed with dichloromethane (120 ml.) and diethyl ether (130 ml.) in turn, and then dried to give p-nitrobenzyl 7-amino-3-cephem-4-carboxylate (7.90 g.), m.p. 182° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04460583
Source datasetuspto-grants-1984_07
ORD IDord-03359a20773f43caa5e54c89962b8830
Source noteuspto-grants-1984_07