HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → n-(4,6-Dimethylpyrimidin-2-yl)-4-[(1-ethyl-1h-benzimidazol-2-ylmethyl)-amino]-benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Sulfamethazine | HCID 5327 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 12408432 | HCID 12408432 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | n-(4,6-Dimethylpyrimidin-2-yl)-4-[(1-ethyl-1h-benzimidazol-2-ylmethyl)-amino]-benzenesulfonamide | HCID 9954705 | — |
Reaction Steps
32.4 mg (0,12 mmol) sulfamethazine and 36 mg (0.18 mmol) 1-ethyl-2-chloromethylbenzimidazole were dissolved in 4 ml methanol. 64 μl (0.44 mmol) triethylamine and catalytic amount of sodium iodide were added to the reaction mixture. Solution was stirred and refluxed overnight. The reaction mixture was then evaporated to dryness, and purified on silica using gradient elution (chloroform to 5% methanol in chloroform) to provide white crystals of the title compound, 10 mg (20%). 1H NMR (DMSO-d6, 500 MHz): 7.68 (2H, m), 7.60 (1H, m), 7.52 (1H, m), 7.22 (1H, m), 7.17 (1H, m), 7.00 (1H, br, s), 6.78 (3H, m), 6.60 (1H, br, s), 4.60 (2H, m), 4.30 (2H, q, 7.2 Hz), 2.18 (6H, s), 1.28 (3H, t, 7.2 Hz); MS (ESI+): m/z 437 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06767909B2 |
| Source dataset | uspto-grants-2004_07 |
| ORD ID | ord-2589bfd48aa7499dbd952b61b4c24db6 |
| Source note | uspto-grants-2004_07 |