HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminothiazole → 4-Iodo-N-(thiazol-2-yl)benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | 4-Iodobenzenesulfonyl chloride | HCID 7399 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 4-Iodo-N-(thiazol-2-yl)benzenesulfonamide | HCID 1019318 | 53.7% |
Reaction Steps
4-Iodobenzenesulfonyl chloride (1.8 g, 6.0 mmol, 1.0 equiv) was added portion-wise to a 0° C. solution of 2-aminothiazole (654 mg, 6.53 mmol, 1.1 equiv) in 4.91 mL of anhydrous pyridine. After addition was complete, the reaction mixture was warmed to ambient temperature. After 3 d, the reaction mixture was concentrated in vacuo. The residue was treated with MeOH and ether to precipitate the product. The solid was collected by filtration, washing with ether, to afford the product as a light brown solid (1.18 g, 49%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08741934B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-7d56d7f57c954631b70c8dff89b7cfc0 |
| Source note | uspto-grants-2014_06 |