HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1905805Generated: November 2, 2026
Pyridine → Benzhydryl 7-amino-3-cephem-4-carboxylate
https://huagongshe.com/reaction/1905805
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | 3-Acetoxy-7beta-phenylacetylaminocepham-4-carboxylic acid diphenylmethyl ester | HCID 13785482 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Isobutanol | HCID 6560 | — |
| Product | Benzhydryl 7-amino-3-cephem-4-carboxylate | HCID 12098365 | 60.8% |
Reaction Steps
To a solution of the above starting material (3a) in dichloromethane (13 parts) under nitrogen are added at -5° to 0° C. pyridine (2 equivalents) and at -30° to -25° C. phosphorus pentachloride (1.7 equivalents). The mixture is stirred at -15° to -10° C. for 4 hours, cooled to -25° to -30° C., mixed with isobutanol (10 parts) cooled at -30° to -20° C., and let stand at 0° to 5° C. overnight. The reaction mixture is cooled to -20° to -25° C., mixed dropwise with triethylamine (10.9 equivalents), and kept at 0° to 5° C. overnight. The reaction mixture is diluted with dichloromethane (20 parts) and ice water (20 parts) and stirred for 20 minutes. The formed organic layer is taken, washed with hydrochloric acid, water, aqueous sodium hydrogen carbonate, and water, dried, and concentrated. The residue is crystallized from ethyl acetate to give 7beta-amino-3-cephem-4-carboxylic acid diphenylmethyl ester (5). Yield: 60.8%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04647658 |
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| Source dataset | uspto-grants-1987_03 |
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| ORD ID | ord-2d708f4cb9db412e9e4c4a63bc6cbfdf |
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| Source note | uspto-grants-1987_03 |
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