HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 3-cyano-4-((tetrahydro-2H-pyran-4-yl)methoxy)benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | (Oxan-4-yl)methanol | HCID 2773573 | — |
| Reactant | 3-Cyano-4-fluorobenzene-1-sulfonamide | HCID 25139897 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-cyano-4-((tetrahydro-2H-pyran-4-yl)methoxy)benzenesulfonamide | HCID 67126413 | — |
Reaction Steps
To (tetrahydro-2H-pyran-4-yl)methanol (0.206 g) in tetrahydrofuran (5 mL) was added sodium hydride (0.284 g) and the reaction stirred at room temperature for 20 minutes. The reaction was cooled to 0° C. and 3-cyano-4-fluorobenzenesulfonamide (0.355 g) in tetrahydrofuran (2 mL) was added dropwise and the reaction was allowed to warm to room temperature. After 3 hours, the reaction was poured into water, made acidic (pH=1) with 1N HCl and extracted with dichloromethane (2×75 mL). The organics were combined, washed with brine (50 mL), dried over magnesium sulfate, filtered and concentrated to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09315488B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-372186fa451e430a81a50ff13ff9fdcb |
| Source note | uspto-grants-2016_04 |