HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → N-(2-chloro-4-sulfamoyl-phenyl)-2-[[4-(8-ethyltetralin-5-yl)-5-(fluoromethyl)-1,2,4-triazol-3-yl]sulfanyl]acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-chloro-N-(2-chloro-4-sulfamoylphenyl)acetamide | HCID 21528830 | — |
| Reactant | HCID 178436513 | HCID 178436513 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(2-chloro-4-sulfamoyl-phenyl)-2-[[4-(8-ethyltetralin-5-yl)-5-(fluoromethyl)-1,2,4-triazol-3-yl]sulfanyl]acetamide | HCID 16728211 | 47% |
Reaction Steps
In a solution of 4-(4-ethyl-5,6,7,8-tetrahydro-naphthalen-1-yl)-5-fluoromethyl-4H-[1,2,4]triazole-3-thiol (85 mg, 0.29 mmol), K2CO3 (44.4 mg, 0.32 mmol) in DMF (2.0 mL) was added 2-chloro-N-(2-chloro-4-sulfamoyl-phenyl)-acetamide (82.6 mg, 0.29 mmol). The reaction mixture was stirred at room temperature for 16 h. Upon the completion of the reaction, H2O (2.0 mL) was added to the reaction and stirred til precipitation occurred and filtered to give solid (73.0 mg, 47% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08481581B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-0037b96765434633a908b2b378f36468 |
| Source note | uspto-grants-2013_07 |