HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591270Generated: November 1, 2026
Trifluoroacetic acid → HCID 141560927, compound
https://huagongshe.com/reaction/1591270
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Anisole | HCID 7519 | — |
| Reactant | HCID 141560930 | HCID 141560930 | — |
| Solvent | Ammonium phosphate, tribasic | HCID 159282 | — |
| Product | HCID 141560927 | HCID 141560927 | 52% |
Reaction Steps
Diphenylmethyl 7-[2-(2-aminothiazol-4-yl)-(Z)-2-methoxyiminoacetamido]-3-(2-amino-3,4-dioxo-1-cyclobutenyl)-3-cephem-4-carboxylate (400 mg) was added to a stirred, cooled (ice/H2O bath) solution of trifluoroacetic acid (6 mL) and anisole (0.5 mL). The cooling bath was removed and the solution stirred for 0.33 hr at ambient temperatures. The solution was concentrated and the residue macerated with methylene chloride to afford a yellow solid. The solid was dissolved in 0.05M (pH 6.5) ammonium phosphate. The solution was applied to a Michel-Miller HPLPLC column (22×300 mm) containing Partisil Prep 40 ODS-3. The column was eluted with 0.05M (pH 6.5) ammonium phosphate/acetonitrile (90:10). The appropriate fractions were combined and the pH lowered to 3.7 with the addition of dilute hydrochloric acid. The solution was concentrated to a volume of 50 mL when the title compound crystallized (155 mg, 52% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05206360 |
|---|
| Source dataset | uspto-grants-1993_04 |
|---|
| ORD ID | ord-abfe16bfb3904c59aad1e2de0791da9a |
|---|
| Source note | uspto-grants-1993_04 |
|---|