HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → N-(5-Iodo-pyridin-2-YL)-4-methyl-benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | 2-Pyridinamine, 5-iodo- | HCID 88579 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N-(5-Iodo-pyridin-2-YL)-4-methyl-benzenesulfonamide | HCID 21772024 | — |
Reaction Steps
p-Toluenesulfonyl chloride (2.00 g, 10.4 mmol) was added to a solution of 5-iodo-2-aminopyridine (2.50 g, 11.4 mmol) in 6 mL of pyridine, and the resultant solution was warmed at 90° C. for 18 h. After cooling to room temperature, the solution was added portionwise to 75 mL of ice-water with stirring. The resultant precipitate was collected, washed with water, and dried in vacuo to afford a pale yellow powder, which was stirred with 20 mL of methanol for several minutes. The solid product was then collected, washed with methanol, and dried in vacuo to provide the title compound as an off-white powder. LC/MS 374.8 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07157490B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-082c0a7fcb6c40b98fc0d69b25098261 |
| Source note | uspto-grants-2007_01 |