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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 844051생성일: 2026년 10월 26일

Mafenide → 2-(3-Cyano-phenoxy)-N-(4-sulfamoyl-benzyl)-nicotinamide

https://huagongshe.com/reaction/844051

반응식

참여 물질

역할이름HCID투입량
반응물MafenideHCID 3998—
반응물DiisopropylethylamineHCID 81531—
반응물Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
반응물2-(3-Cyano-phenoxy)-nicotinic acidHCID 12849335—
용매DimethylformamideHCID 6228—
생성물2-(3-Cyano-phenoxy)-N-(4-sulfamoyl-benzyl)-nicotinamideHCID 2261207340.8%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06380218B1
출처 데이터셋uspto-grants-2002_04
ORD IDord-95b0ae0cc4cf4406b73bb5dc768e9860
출처 메모uspto-grants-2002_04