HuagongsheHuagongshe Chemistry Print Report · For research reference only
(Oxan-4-yl)methanol → 5-bromo-6-((4-fluorotetrahydro-2H-pyran-4-yl)methoxy)pyridine-3-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (Oxan-4-yl)methanol | HCID 2773573 | — |
| Reactant | 5-Bromo-6-chloropyridine-3-sulfonamide | HCID 4730022 | — |
| Reactant | 4-Fluoro-3-nitrobenzenesulfonamide | HCID 16782487 | — |
| Product | 5-bromo-6-((4-fluorotetrahydro-2H-pyran-4-yl)methoxy)pyridine-3-sulfonamide | HCID 67126452 | — |
Reaction Steps
The title compound was prepared by substituting (4-fluorotetrahydro-2H-pyran-4-yl)methanol for (tetrahydro-2H-pyran-4-yl)methanol and 5-bromo-6-chloropyridine-3-sulfonamide for 4-fluoro-3-nitrobenzenesulfonamide in EXAMPLE 24A.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09174982B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-3133bf26bb2c4420a2274e10c29d6f31 |
| Source note | uspto-grants-2015_11 |