HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Bromo-5-(trifluoromethyl)benzenesulfonyl chloride → 3-Aminomethyl-N-tert-butyl-5-trifluoromethyl-benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Bromo-5-(trifluoromethyl)benzenesulfonyl chloride | HCID 2778610 | — |
| Reactant | 5-Aminomethyl-N-tert-butyl-2-fluoro-benzenesulfonamide | HCID 28716369 | — |
| Product | 3-Aminomethyl-N-tert-butyl-5-trifluoromethyl-benzenesulfonamide | HCID 67161162 | — |
Reaction Steps
3-Aminomethyl-N-tert-butyl-5-trifluoromethyl-benzenesulfonamide was synthesized in a manner analogous to 5-aminomethyl-N-tert-butyl-2-fluoro-benzenesulfonamide in Example 3, using 3-bromo-5-(trifluoromethyl)benzene-1-sulfonyl chloride in place of 5-chloro-2-fluorobenzene-1-sulfonyl chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08536187B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-3d5058b4f7644799a83183f49e5ee90b |
| Source note | uspto-grants-2013_09 |