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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | p-Nitrobenzyl 7-phenylacetamido-3-cephem-4-carboxylate | HCID 70362156 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | p-Nitrobenzyl 7-amino-3-cephem-4-carboxylate | HCID 12775080 | 101.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04460583 |
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| Source dataset | uspto-grants-1984_07 |
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| ORD ID | ord-03359a20773f43caa5e54c89962b8830 |
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| Source note | uspto-grants-1984_07 |
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