HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 974871Generated: October 25, 2026
Trifluoroacetic acid → HCID 178502776, compound
https://huagongshe.com/reaction/974871
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Diisopropyl Ether | HCID 7914 | — |
| Reactant | O-benzhydryl (6R)-3-(1,3-benzoxazol-2-yl)-7-[[(2Z)-2-methoxyimino-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carbothioate | HCID 172974451 | — |
| Solvent | Anisole | HCID 7519 | — |
| Product | HCID 178502776 | HCID 178502776 | — |
Reaction Steps
A 272 mg portion of diphenylmethyl 7-{(Z)-2-(2-tritylaminothiazol-4-yl)-2-methoxyiminoacetamido }-3-(benzoxazol-2-yl)thio-3-cephem-4-carboxylate was dissolved in 1.4 ml of anisole. Under cooling on an ice bath, the resulting solution was mixed with 2.7 ml of trifluoroacetic acid and stirred for 30 minutes at the same temperature. The resulting reaction mixture was added dropwise to 14 ml of diisopropyl ether, and the formed precipitate was recovered by filtration and dried. The thus dried product was suspended in 3 ml of distilled water, and the suspension was adjusted to pH 7 with saturated sodium bicarbonate aqueous solution. Thereafter, this solution was chromatographed using 10 ml of HP-20 resin and freeze-dried to obtain 73 mg of the title compound as a sodium salt (yield, 46%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05607927 |
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| Source dataset | uspto-grants-1997_03 |
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| ORD ID | ord-926b3650fe394946bc52804a86bef27e |
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| Source note | uspto-grants-1997_03 |
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