HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 5-Bromo-6-chloropyridine-3-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 5-Bromo-6-chloropyridine-3-sulfonyl chloride | HCID 2793626 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-Bromo-6-chloropyridine-3-sulfonamide | HCID 4730022 | — |
Reaction Steps
5-Bromo-6-chloropyridine-3-sulfonyl chloride (8.2 g) in methanol (20 mL) was cooled to 0° C. To this solution was added 7N NH3 in methanol (80 mL). The reaction mixture was stirred overnight. The solvent was removed at low temperature, and the residue was partitioned between ethyl acetate and water. The aqueous layer was extracted with ethyl acetate three times. The combined organic layers were washed with brine, dried (MgSO4), filtered, and concentrated. The residue was purified by flash column chromatography on silica gel to give the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09029404B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-a11b05351f2d40da8332d9b9d459e610 |
| Source note | uspto-grants-2015_05 |