HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → 4-[5-Amino-1-(6-phenoxy-benzothiazol-2-yl)-1H-[1,2,4]triazol-3-ylamino]-benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 5-Amino-3-(4-sulfamoyl-phenylamino)-[1,2,4]triazole-1-carbothioic acid (4-phenoxy-phenyl)-amide | HCID 58976467 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-[5-Amino-1-(6-phenoxy-benzothiazol-2-yl)-1H-[1,2,4]triazol-3-ylamino]-benzenesulfonamide | HCID 58976411 | 7% |
Reaction Steps
Bromine (7 μl, 1 equivalent) was added to a stirred suspension of 5-amino-3-(4-sulfamoyl-phenylamino)-[1,2,4]triazole-1-carbothioic acid (4-phenoxy-phenyl)-amide in dichloromethane (3 ml). The reaction mixture was stirred at room temperature for 18 hours. A solution of bromine (7 μl) in acetic acid (1 ml) was then added to push the reaction to completion: the reaction mixture was stirred for a further four hours. A white solid precipitated and was removed by filtration to afford the title compound (5 mg; 7% yield). 1H NMR (400 MHz, DMSO-d6) 7.05-7.20 (8H, m), 7.35-7.50 (4H, m), 7.70-7.75 (2H, d), 7.80-7.85 (2H, d), 9.90-9.95 (1H, s); MS (ES+) m/e=480
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07279469B2 |
| Source dataset | uspto-grants-2007_10 |
| ORD ID | ord-20b317f8945847fb9136b0fa4d29ab08 |
| Source note | uspto-grants-2007_10 |