HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2,4-Thiadiazol-5-amine, 3-phenyl- → 3,4-Dimethoxy-n-[3-(phenyl)-1,2,4-thiadiazol-5-yl]benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2,4-Thiadiazol-5-amine, 3-phenyl- | HCID 28561 | — |
| Reactant | 3,4-Dimethoxybenzenesulfonyl chloride | HCID 2734183 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 3,4-Dimethoxy-n-[3-(phenyl)-1,2,4-thiadiazol-5-yl]benzenesulfonamide | HCID 24993888 | 14.4% |
Reaction Steps
3-Phenyl-1,2,4-thiadiazol-5-amine (326 mg, 1.84 mmol) was dissolved in dry pyridine (10 mL). Then 3,4-dimethoxybenzenesulfonyl chloride (529 mg, 2.23 mmol) was added. The solution was stirred at room temperature under Argon. After 46 h, the pyridine was removed in vacuo and flashed off with toluene. The residue was partitioned between EtOAc and 1M NaOH. The organic phase was washed with 1M NaOH until no turbidity was observed on rectification of a small sample. The alkaline phase was made acidic (˜pH 3) with 1M HCl and extracted with EtOAc. After drying over Na2SO4, the solvent was removed in vacuo to give a solid (100 mg) which was crystallized from EtOAc. Yield was 29.3 mg; mp 170-171° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08466182B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-f30479d44bf84d69896b857a12ee40c3 |
| Source note | uspto-grants-2013_06 |