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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 447807생성일: 2026년 10월 24일

Potassium Carbonate → 5-Chloro-2-imino-1-[3-(methylsulfamoyl)benzyl]-1,2-dihydropyridine-3-carboxamide hydrochloride

https://huagongshe.com/ko/reaction/447807

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물2-Cyano-2-(3,4-dichloro-5(2H)-oxo-2-furyl)acetamideHCID 541792—
반응물3-(Aminomethyl)-N-methylbenzene-1-sulfonamideHCID 16785597—
용매EthanolHCID 702—
생성물5-Chloro-2-imino-1-[3-(methylsulfamoyl)benzyl]-1,2-dihydropyridine-3-carboxamide hydrochlorideHCID 6696989932.6%

반응 조건

온도70 °C

반응 단계

(Step 2) To a suspension of 2-cyano-2-(3,4-dichloro-5-oxo-2,5-dihydrofuran-2-yl)acetamide (0.28 g) and 3-(aminomethyl)-N-methylbenzenesulfonamide obtained in Step 1 (0.36 g) in ethanol (10 ml) was added potassium carbonate (0.25 g) at room temperature, and the mixture was stirred overnight at 70° C. The reaction solution was filtered through celite. The solvent was evaporated under reduced pressure. The residue was purified by basic silica gel column chromatography (ethyl acetate:hexane=7:3→1:0). 4N Hydrochloride-ethyl acetate solution (1 ml) was added to the obtained yellow oil, and the precipitated crystals were collected by filtration, and recrystallized to give the title compound (76 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08481569B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-6b65ed388688401c8de919d0705caa2b
출처 메모uspto-grants-2013_07