Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Phosphorus trichloride | HCID 24387 | — |
| Reactant | HCID 88675696 | HCID 88675696 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 88675687 | HCID 88675687 | 89% |
Reaction Steps
A mixture of benzhydryl 7-(2-phenylacetamido)-3-[1-(2-propynyl)-1H-tetrazol-5-yl]thiomethyl-3-cephem-4-carboxylate-1-oxide (9.3 g) and dry N,N-dimethylformamide (93 ml) was cooled to -30° C. and thereto was added phosphorus trichloride (3.9 g). The resulting solution was stirred for 40 minutes at -30° C. The reaction mixture was allowed to warm to ambient temperature, added to water (150 ml) and then extracted with ethyl acetate (×3). The extracts were combined, washed successively with a saturated aqueous solution of sodium bicarbonate (×2) and water (×3), dried over magnesium sulfate, treated with activated charcoal and then evaporated. The residue was pulverized in a mixture of isopropyl ether and n-hexane, collected by filtration, washed with n-hexane and then dried to give benzhydryl 7-(2-phenylacetamido)-3-[1-(2-propynyl)-1H-tetrazol-5-yl]thiomethyl-3-cephem-4-carboxylate (8.07 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04563450 |
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| Source dataset | uspto-grants-1986_01 |
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| ORD ID | ord-e5693c814f5d49bd8ab29818d19de9d4 |
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| Source note | uspto-grants-1986_01 |
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