HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfamethazine → N-[4-(4,6-Dimethylpyrimidin-2-ylsulfamoyl)-phenyl]-2-(2-methoxyphenyl)-acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfamethazine | HCID 5327 | — |
| Reactant | 2-Methoxyphenylacetic acid | HCID 7134 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Diisopropylcarbodiimide | HCID 12734 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | N-[4-(4,6-Dimethylpyrimidin-2-ylsulfamoyl)-phenyl]-2-(2-methoxyphenyl)-acetamide | HCID 23504900 | 40% |
Reaction Steps
2-Methoxyphenylacetic acid (33 mg, 0.20 mmol) and sulfamethazine (55 mg, 0.20 mmol) were dissolved in 4 ml of chloroform. Triethylamine (70 μl, 0.55 mmol) and diisopropylcarbodiimide (50 μl, 0.20 mmol) were added to the reaction mixture. Solution was stirred and refluxed overnight. The reaction mixture was then evaporated to dryness, washed with water and purified on silica using gradient elution (chloroform to 2% methanol in chloroform) to obtain white crystals with the yield of 40%. 1H NMR (CDCl3, 500 MHz): 8.04 (2H, m), 7.54 (2H, m), 7.30 (2H, m), 6.98 (2H, m), 6.60 (1H, s), 3.95 (3H, s), 3.72 (2H, s), 2.33 (6H, s); MS (ESI+): m/z 449 (M+Na)+, 427 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06767909B2 |
| Source dataset | uspto-grants-2004_07 |
| ORD ID | ord-433da962c43a4fbf8a0b104ef2722b91 |
| Source note | uspto-grants-2004_07 |