Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Sulfamethazine → N-[4-(4,6-Dimethylpyrimidin-2-ylsulfamoyl)-phenyl]-2-(2-methoxyphenyl)-acetamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Sulfamethazine | HCID 5327 | — |
| 반응물 | 2-Methoxyphenylacetic acid | HCID 7134 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Diisopropylcarbodiimide | HCID 12734 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 생성물 | N-[4-(4,6-Dimethylpyrimidin-2-ylsulfamoyl)-phenyl]-2-(2-methoxyphenyl)-acetamide | HCID 23504900 | 40% |
반응 단계
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)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06767909B2 |
| 출처 데이터셋 | uspto-grants-2004_07 |
| ORD ID | ord-433da962c43a4fbf8a0b104ef2722b91 |
| 출처 메모 | uspto-grants-2004_07 |