HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Topiramate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Chlorosulfamic acid | HCID 24499 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 131714623 | HCID 131714623 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Topiramate | HCID 5284627 | — |
Reaction Steps
To a cold solution (-4° C.) of 2,3:4,5-di-O-isopropylidene-β-fructopyranose (75 g, 0.29 mol) in DMF (725 ml) was added 50% oily sodium hydride (16.34 g, 0.34 mol as NaH). After stirring for 90 min, sulfamoyl chloride (54.9 g, 0.48 mol) was added and the stirring continued for an additional 3.5 hr at that temperature. The reaction mixture was poured into cold water and extracted with toluene. The organic layer was dried (Na2SO4) and the solvents removed under vacuum to give a syrup which crystallized immediately. Recrystallization from ethylacetate/hexane gave pure 2,3:4,5-bis-O-methylethylidene)-β-D-fructopyranose sulfamate, mp 125°-126° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04582916 |
| Source dataset | uspto-grants-1986_04 |
| ORD ID | ord-8404ca2c560a48afbe9e94cf58cab845 |
| Source note | uspto-grants-1986_04 |