HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → 7beta-Amino-3-(3-formamido-2-methyl-1-pyrazolio)methyl-3-cephem-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Anisole | HCID 7519 | — |
| Reactant | Diisopropyl Ether | HCID 7914 | — |
| Reactant | Benzhydryl 7beta-tert-butoxycarbonylamino-3-(3-formamido-2-methyl-1-pyrazolio)methyl-3-cephem-4-carboxylate iodide | HCID 10628738 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 7beta-Amino-3-(3-formamido-2-methyl-1-pyrazolio)methyl-3-cephem-4-carboxylate | HCID 10806845 | 168.1% |
Reaction Steps
To a solution of benzhydryl 7β-tert-butoxycarbonylamino-3-(3-formamido-2-methyl-1-pyrazolio)methyl-3-cephem-4-carboxylate iodide (20.9 g) and anisole (20 ml) in methylene chloride (40 ml) was added dropwise trifluoroacetic acid (40 ml) under ice-cooling. After being stirred for 1.5 hours at ambient temperature, the mixture was poured into a mixture of diisopropyl ether (300 ml) and ethyl acetate (300 ml). The resultant precipitate was collected by filtration to give di(trifluoroacetic acid) salt of 7β-amino-3-(3-formamido-2-methyl-1-pyrazolio)methyl-3-cephem-4-carboxylate (16.20 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05108997 |
| Source dataset | uspto-grants-1992_04 |
| ORD ID | ord-71325088a3a44c2cad32c123248cb4e3 |
| Source note | uspto-grants-1992_04 |