Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Diisopropyl Ether | HCID 7914 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | Benzhydryl 7-phenylacetamido-3-(2,2-dibromovinyl)-2-cephem-4-carboxylate | HCID 88600993 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 88601078 | HCID 88601078 | 97.8% |
Reaction Steps
To a suspension of phosphorus pentachloride (13.74 g) in dichloromethane (150 ml) was dropwise added pyridine (5.34 ml) at -15° to -10° C. under stirring which was continued at the same temperature for 30 minutes. To the above mixture was added benzhydryl 7-phenylacetoamido-3-(2,2-dibromovinyl)-2-cephem-4-carboxylate (29.4 g) at -5° C. After the reaction mixture was stirred at -5° for 1.5 hours, methanol (26.62 ml) was dropwise added to the reaction mixture under cooling at -20° and the mixture was stirred at -20° C. to -5° C. for 1.5 hours. Then water (30 ml) was added to the reaction mixture under ice-cooling. After the reaction mixture was stirred for an hour at the same temperature, diisopropylether (100 ml) was added to the reaction mixture at 0° C. The resultant precipitates were collected by filtration and washed in turn with water and diisopropyl ether to give benzhydryl 7-amino-3-(2,2-dibromovinyl)-2-cephem-4-carboxylate hydrochloride (25.23 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04609730 |
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| Source dataset | uspto-grants-1986_09 |
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| ORD ID | ord-f5ff54d63f264e73a94f49d38810e941 |
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| Source note | uspto-grants-1986_09 |
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