Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 88523165 | HCID 88523165 | — |
| Product | HCID 88523025 | HCID 88523025 | — |
Reaction Steps
Benzhydryl 7-[(Z)-2-(2-tritylaminothiazol-4-yl)-2-trityloxyiminoacetamido]-3-[(Z)-2-(5-methyl-1,2,3-thiadiazol-4-yl)vinyl]-3-cephem-4-carboxylate (0.5 g, 0.4 mmol) was stirred at room temperature for 2 hours by addition of formic acid (5 ml). Concentrated hydrochloric acid (40 μl) was added to the reaction solution and it was stirred at room temperature for 1 hour. The reaction solution was concentrated under reduced pressure and then the residue was cleansed with ether thereby a powdered product was obtained. This one was dissolved in aqueous sodium bicarbonate solution and purified by HP-20 column chromatography thereby sodium 7-[(Z)-2-(2-aminothiazol-4-yl)-2-hydroxyiminoacetamido]-3-[(Z)-2-(5-methyl-1,2,3-thiadiazol-4-yl)vinyl]-3-cephem-4-carboxylate (0.13 g) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05073551 |
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| Source dataset | uspto-grants-1991_12 |
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| ORD ID | ord-f67fb7c7a9c240ce9ba37d78d0662e8e |
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| Source note | uspto-grants-1991_12 |
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