HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) → N-(5-chloro-3-methoxypyrazin-2-yl)-4'-hydroxy-N-(isobutoxycarbonyl)-2-biphenylsulphonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) | HCID 466102 | — |
| Reactant | HCID 53756881 | HCID 53756881 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(5-chloro-3-methoxypyrazin-2-yl)-4'-hydroxy-N-(isobutoxycarbonyl)-2-biphenylsulphonamide | HCID 22911291 | 97.8% |
Reaction Steps
N-(5-Chloro-3-methoxypyrazin-2-yl)- N-(isobutoxycarbonyl)-4'-[2-(2 H)-tetrahydropyranyloxy]-2-biphenylsulphonamide (1.15 g) and pyridinium-p-toluenesulphonate (50 mg) in ethanol (50 ml) was heated at 60° C. for 3 hours. Volatile material was removed by evaporation and the residue was triturated with etherexane (1:1 v/v) to give N-(5-chloro-3-methoxypyrazin-2-yl)-4'-hydroxy- N-(isobutoxycarbonyl)-2-biphenylsulphonamide (0.96 g), m.p. 175°-177° C.; microanalysis found: C, 53.9; H, 4.8; N, 8.2%; C21H22C1N3O6 requires: C, 53.7; H, 4.5; N, 8.5%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05668137 |
| Source dataset | uspto-grants-1997_09 |
| ORD ID | ord-2a231f1f8cee4e5bb2d0d4d0d041e51e |
| Source note | uspto-grants-1997_09 |