HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2253986Generated: November 1, 2026
Trifluoroacetic acid → HCID 178508509, compound
https://huagongshe.com/reaction/2253986
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 178475464 | HCID 178475464 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178508509 | HCID 178508509 | 138% |
Reaction Steps
After 0.22 g of the compound obtained in Example 6 (7) was added to 25 ml of trifluoroacetic acid, the mixture was stirred at room temperature for an hour. The reaction mixture was cooled to 5° C. and 6 ml of water was added thereto. After stirring at 5° C., the temperature was reverted to room temperature followed by stirring for 2 hours. The solvent was distilled off under reduced pressure and ether was added to the residue to make powders. To the powders was added 100 ml of water and then 0.20 g of sodium hydrogencarbonate. The mixture was adsorbed to DIAION HP20 followed by elution with water-methanol. The fractions containing the desired product were collected. After concentration, the concentrate was freeze dried to give 90 mg (52.9%) of trisodium 7β-[(Z)-2-(2-amino-4-thiazolyl)-2-[[(R S)-(carboxy)(3-pyridyl)methoxy]imino]acetamido]-3-[[(4-carboxy-3-hydroxy-5-isothiazolyl)thio]methyl]-3-cephem-4-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05233035 |
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| Source dataset | uspto-grants-1993_08 |
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| ORD ID | ord-1839717dc7024c4db9bd86de519c8834 |
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| Source note | uspto-grants-1993_08 |
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