HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 4-(4-Chloro-phenoxy)-N-(2,5-dibromo-pyridin-3-yl)-benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 4-(4-Chlorophenoxy)benzene-1-sulfonyl chloride | HCID 2757750 | — |
| Reactant | 2,5-Dibromopyridin-3-amine | HCID 19387532 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(4-Chloro-phenoxy)-N-(2,5-dibromo-pyridin-3-yl)-benzenesulfonamide | HCID 86619933 | — |
Reaction Steps
To a solution of 2,5-dibromo-3-aminopyridine (0.51 g, 2.0 mmol) and 4-(4-chloro-phenoxy)-benzenesulfonyl chloride (0.76 g, 2.0 mmol) in dry CH2Cl2 (10 mL) was added pyridine (1 mL) at 0 C. The resulting mixture was allowed to warm to room temperature and stirred until TCL showed the completion of the reaction. The reaction mixture was diluted with CH2Cl2 and washed with aqueous HCl solution. After the pyridine was neutralized, the organics were washed with water, brine and dried over anhydrous Na2SO4. The filtration (Celite) and concentration under vacuo gave a crude material, which was purified by silica column (30% EtOAc/hexanes). MS: 516, 518 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07803793B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-d44ecc8be2504abf90045b8b7f55bda9 |
| Source note | uspto-grants-2010_09 |