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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 447803생성일: 2026년 10월 24일

Water → 5-Chloro-1-(5-chloro-2-(methylsulfonyl)benzyl)-2-imino-1,2-dihydropyridine-3-carboxamide hydrochloride

https://huagongshe.com/ko/reaction/447803

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참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물DiisopropylethylamineHCID 81531—
반응물2-Cyano-2-(3,4-dichloro-5(2H)-oxo-2-furyl)acetamideHCID 541792—
반응물HCID 66969896HCID 66969896—
용매EthanolHCID 702—
생성물5-Chloro-1-(5-chloro-2-(methylsulfonyl)benzyl)-2-imino-1,2-dihydropyridine-3-carboxamide hydrochlorideHCID 6697008689.9%

반응 조건

온도70 °C

반응 단계

(Step 4) To a suspension of 2-cyano-2-(3,4-dichloro-5-oxo-2,5-dihydrofuran-2-yl)acetamide (0.28 g) and 1-[5-chloro-2-(methylsulfonyl)phenyl]methanamine hydrochloride obtained in Step 3 (0.26 g) in ethanol (3 ml) was added N,N-diisopropylethylamine (0.44 ml) at room temperature, and the resulting mixture was heated under reflux for 4 hr. The reaction mixture was treated with water and stirred at 70° C. for 1 hr. After cooling to room temperature, the precipitate was collected by filtration and dried. The precipitate was suspended in methanol, and treated with a 2 M hydrogen chloride-methanol solution (0.3 ml). The resulting mixture was stirred at room temperature overnight. The precipitate was collected by filtration and dried to give the title compound (0.22 g) as white crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08481569B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-56ed163206734d0fbcd7db865f382310
출처 메모uspto-grants-2013_07