Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | HCID 131711504 | HCID 131711504 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 131711505 | HCID 131711505 | 29.6% |
Reaction Steps
A mixture of 610 mg of the product of Example 8 and 3 ml of 50% aqueous formic acid was heated at 60° C. for 15 minutes and 4 ml of water were added. The mixture was stirred and vacuum filtered. The filtrate was rinsed with water and concentrated to dryness under reduced pressure. The residue was taken up in water and was effloresced. The mixture was vacuum filtered and the product was rinsed to obtain 120 mg of 3-acetoxymethyl-7-[2-(2-amino-4-thiazolyl)-2-(2-propenyl) oxyiminoacetamido]-ceph-3-eme-4-carboxylic acid with a melting point of about 160° C. and a syn configuration.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04152432 |
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| Source dataset | uspto-grants-1979_05 |
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| ORD ID | ord-76b43029be4949dfa36f0549c9452630 |
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| Source note | uspto-grants-1979_05 |
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