HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720707Generated: October 29, 2026
Water → 4-[5-(4-Bromo-phenyl)-3-methyl-[1,2,4]triazole-1-yl]-benzenesulfonamide
https://huagongshe.com/reaction/720707
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Hydrazinylbenzenesulfonamide hydrochloride | HCID 2794567 | — |
| Reactant | N-(1-ethoxy-ethylidene)-4-bromo-benzamide | HCID 21894671 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-[5-(4-Bromo-phenyl)-3-methyl-[1,2,4]triazole-1-yl]-benzenesulfonamide | HCID 10150664 | 73% |
Reaction Steps
N-(1-ethoxy-ethylidene)-4-bromo-benzamide 565 mg(2.09 mmol) was dissolved in a mixed solvent of dichloromethane 20 ml and methanol 10 ml, and 4-hydrazinobenzenesulfonamide hydrochloride 515 mg (2.23 mmol) was added to the solution. Then, triethylamine 0.35 ml (2.51 mmol) was slowly added dropwise at room temperature for 10 minutes and stirred for 8 hours. After completing the reaction, water 20 ml was added to the reacting solution and extracted two times with dichloromethane, and then, the collected organic layer was washed with saturated brine. The organic layer was dried with anhydrous magnesium sulfate, filtered and concentrated under reduced pressure, and the resulting product was re-crystallized in acetone and hexane phase. As a result, 4-[5-(4-bromo-phenyl)-3-methyl-[1,2,4]triazole-1-yl]-benzenesulfonamide (600 mg, yield: 73%) was obtained as a solid phase.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07135572B2 |
|---|
| Source dataset | uspto-grants-2006_11 |
|---|
| ORD ID | ord-b07d861516234b76865ffd00d1b69c56 |
|---|
| Source note | uspto-grants-2006_11 |
|---|