Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | HCID 88675687 | HCID 88675687 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 88675660 | HCID 88675660 | 94.7% |
Reaction Steps
A mixture of phosphorus pentachloride (5.3 g) in methylene chloride (80 ml) was cooled to 5° C. and thereto was added pyridine (2.0 g). The mixture was stirred for 30 minutes at room temperature and then cooled to 5° C. and thereto was added benzhydryl 7-(2-phenylacetamido)-3-[1-(2-propynyl)-1H-tetrazol-5-yl]thiomethyl-3-cephem-4-carboxylate (8.0 g) to give a homogeneous solution. The obtained solution was stirred for 30 minutes at 5° C. and added to methanol (40.2 g) precooled to -30° C. The resulting mixture was stirred for 30 minutes without external cooling. The reaction mixture was evaporated and to the residue were added ethyl acetate and water. The mixture was adjusted to pH 7.0 with a saturated aqueous solution of sodium carbonate. The ethyl acetate layer was separated, washed with water (x3), dried over magnesium sulfate, treated with activated charcoal and evaporated under reduced pressine to give benzhydryl 7-amino-3-[ 1-(2-propynyl)-1H-tetrazol-5-yl]thiomethyl-3-cephem-4-carboxylate (6.17 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04405617 |
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| Source dataset | uspto-grants-1983_09 |
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| ORD ID | ord-3dcd589e11f947d3b7a0bbd4d6ae198f |
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| Source note | uspto-grants-1983_09 |
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