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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 44338생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/44338

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 5745690290.1%

반응 단계

To a solution of 2-amino-4,5-dimethylthiophene-3-carbonitrile (example 4b) (25 g, 164.5 mmol) in 1.4-dioxane (600 mL) was added benzoyl isocyanate (24.2 g, 164.5 mmol). The reaction mixture was then stirred at room temperature under nitrogen overnight. The precipitate was collected by filtration, washed with 1.4-dioxane (20 mL×3), and dried under vacuum at 40° C. for 3 hours to give N-(3-cyano-4,5-dimethylthiophen-2-ylcarbamoyl)benzamide (44.35 g, 90%) as a white solid. 1H NMR (400 MHz, DMSO-d6) δ2.10 (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 번호US08541421B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-8d622ce8eff24443b3fa8ee750c7b985
출처 메모uspto-grants-2013_09