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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1884818생성일: 2026년 10월 26일

Sodium Iodide → n-(4,6-Dimethylpyrimidin-2-yl)-4-[(1-ethyl-1h-benzimidazol-2-ylmethyl)-amino]-benzenesulfonamide

https://huagongshe.com/reaction/1884818

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물SulfamethazineHCID 5327—
반응물TriethylamineHCID 8471—
반응물1H-Benzimidazole, 2-(chloromethyl)-1-ethyl-HCID 12408432—
용매MethanolHCID 887—
생성물n-(4,6-Dimethylpyrimidin-2-yl)-4-[(1-ethyl-1h-benzimidazol-2-ylmethyl)-amino]-benzenesulfonamideHCID 9954705—

반응 단계

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)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06767909B2
출처 데이터셋uspto-grants-2004_07
ORD IDord-2589bfd48aa7499dbd952b61b4c24db6
출처 메모uspto-grants-2004_07