HuagongsheHuagongshe Chemistry Print Report · For research reference only
Erythromycin → Flurithromycin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Erythromycin | HCID 12560 | — |
| Reactant | N-Fluorobenzenesulfonimide | HCID 588007 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Flurithromycin | HCID 71260 | 18.2% |
Reaction Steps
Erythromycin A (5 g, 6.813 mmole) was dissolved in glacial acetic acid (20 mL) at room temperature and stirred for 2 hours. N-fluorobenzenesulfonimide (2.2 g, 6.813 mmole) dissolved in THF (4 mL) was added and stirring continued for an additional 18 hours at 22° C. The reaction was worked up in the same manner as Example 1 to afford only 0.93 g (7% yield) of crude flurithromycin.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05552533 |
| Source dataset | uspto-grants-1996_09 |
| ORD ID | ord-3b606532f3ea45998210d765f36f2942 |
| Source note | uspto-grants-1996_09 |