HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → 5-bromo-2-chloro-N-(5-trifluoromethyl-pyridin-2-yl)-benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | 2-Amino-5-(trifluoromethyl)pyridine | HCID 735862 | — |
| Reactant | 5-Bromo-2-chloro-N-phenyl-benzenesulfonamide | HCID 68724727 | — |
| Product | 5-bromo-2-chloro-N-(5-trifluoromethyl-pyridin-2-yl)-benzenesulfonamide | HCID 68725769 | — |
Reaction Steps
The titled compound is prepared as described for 5-Bromo-2-chloro-N-phenyl-benzenesulfonamide (Intermediate F, step 2), by replacing aniline in this procedure with 5-trifluoromethyl-pyridin-2-ylamine
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08263585B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-5562a05665ca41c389253e0e1450a95c |
| Source note | uspto-grants-2012_09 |