Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Mafenide → 2-(3-Cyano-phenoxy)-N-(4-sulfamoyl-benzyl)-nicotinamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Mafenide | HCID 3998 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate | HCID 151348 | — |
| 반응물 | 2-(3-Cyano-phenoxy)-nicotinic acid | HCID 12849335 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 2-(3-Cyano-phenoxy)-N-(4-sulfamoyl-benzyl)-nicotinamide | HCID 22612073 | 40.8% |
반응 단계
To a solution of 2-(3-Cyano-phenoxy)-nicotinic acid (0.140 g 0.600 mmole), BOP (0.260 grams, 0.600 mmole) and DIEA (0.310 μl, 1.8 mmole) in dimethylformamide (5 ml) was added 4-Aminomethyl-benzenesulfonamide (0.135 grams, 0.600 mmole) and stirred at room temperature over night. The reaction was quenched with water and extracted with ethyl acetate. The combined organics were washed with alternating portions of 5% citric acid and sat'd bicarb, dried over Na2SO4, filtered and concentrated to a product which was recrystalized from ethyl acetate to give a white solid (0.100 g). M.P. 179-180° C.; Anal. calcd. for C20H16N4O4S; C, 58.81; H, 3.95; N, 13.72. Found: C, 57.47; H, 4.15; N. 13.45.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06380218B1 |
| 출처 데이터셋 | uspto-grants-2002_04 |
| ORD ID | ord-95b0ae0cc4cf4406b73bb5dc768e9860 |
| 출처 메모 | uspto-grants-2002_04 |