HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Luxabendazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Fluorobenzenesulfonyl chloride | HCID 9588 | — |
| Reactant | Methyl 5-hydroxybenzimidazol-2-ylcarbamate | HCID 115152 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Luxabendazole | HCID 72019 | — |
Reaction Steps
2.8 ml of triethylamine are added dropwise, with stirring, to 2.07 g of methyl 5-hydroxybenzimidazole-2-carbamate and 1.94 g of 4-fluorobenzenesulfonyl chloride at about 10° C. The mixture is then stirred at room temperature for 2 h, 100 ml of 2N acetic acid are added while cooling, and the resulting precipitate is filtered off with suction, washed with water and dried. Melting point 236° C., decomposition, from dimethylformamide/methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04639463 |
| Source dataset | uspto-grants-1987_01 |
| ORD ID | ord-d0b27162300f42dea1d082bb33dc2d64 |
| Source note | uspto-grants-1987_01 |