HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1358914Generated: November 4, 2026
Trifluoroacetic acid → HCID 86585656, compound
https://huagongshe.com/reaction/1358914
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | HCID 86585657 | HCID 86585657 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86585656 | HCID 86585656 | — |
Reaction Steps
To a solution of (7R)-7-[2-(2-amino-5-chloro-thiazol-4-yl)-2-trityloxyiminoacetylamino ]-3-(5-amino-[1,3,4]thiadiazol-2-ylsulfanyl)-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester (150 mg, 0.17 mmol) in dichloromethane (7.5 mL) was added triethylsilane (1.5 mL). The mixture was cooled to 0° C. and trifluoroacetic acid (7.5 mL) was added. After 2 hr at 0° C. the reaction mixture was concentrated under vacuum and disopropyl ether was added to the oily residue. The title compound precipitated and was filtered, washed with additional diisopropyl ether and dried under vacuum (85 mg, 65%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06599893B2 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-a7e8039dde2b4566948e5386ad4df3d2 |
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| Source note | uspto-grants-2003_07 |
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