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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 471634생성일: 2026년 10월 25일

Benzoyl isocyanate → N-(3-cyano-4,5-dimethylthiophen-2-ylcarbamoyl)benzamide

https://huagongshe.com/reaction/471634

반응식

참여 물질

역할이름HCID투입량
반응물Benzoyl isocyanateHCID 78210—
반응물2-Amino-4,5-dimethyl-thiophene-3-carbonitrileHCID 290236—
용매1,4-DioxaneHCID 31275—
생성물N-(3-cyano-4,5-dimethylthiophen-2-ylcarbamoyl)benzamideHCID 5745690284.7%

반응 단계

To a solution of 2-amino-4,5-dimethylthiophene-3-carbonitrile (1680 g, 11.04 mol) in 1,4-dioxane (42 L) was added benzoylisocyanate (1624 g, 11.04 mol). The reaction mixture was then stirred at room temperature under nitrogen overnight. The resulting precipitate was collected by filtration, washed with 1,4-dioxane (3×1.7 l) and heptane (3×1.7 L), and dried under vacuum overnight to give N-(3-Cyano-4,5-dimethylthiophen-2-ylcarbamoyl)benzamide as a white solid (2800 g, 84.7% yield). 1H NMR (400 MHz, DMSO-d6) δ 2.10 (s, 3H), 2.24 (s, 3H), 7.52-7.56 (m, 2H), 7.64-7.69 (m, 1H), 8.01-8.03 (m, 2H), 11.57 (brs, 1H), 12.05 (brs, 1H). MS 300 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08633186B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-2a967f5d6e1a4e03a619985ce60fc982
출처 메모uspto-grants-2014_01