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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 499059생성일: 2026년 10월 24일

Acetonitrile → 2-Chloro-N-(4-(4,6-dichloropyrimidin-2-ylthio)phenyl)benzamide

https://huagongshe.com/ko/reaction/499059

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물TriethylamineHCID 8471—
반응물4,6-Dichloro-2-(methylsulfonyl)pyrimidineHCID 239685—
반응물2-chloro-N-(4-mercaptophenyl)benzamideHCID 27137419—
용매WaterHCID 962—
생성물2-Chloro-N-(4-(4,6-dichloropyrimidin-2-ylthio)phenyl)benzamideHCID 5942079774%

반응 조건

온도0 °C

반응 단계

A 250 mL round bottom flask was charged with 4,6-dichloro-2-methanesulfonylpyrimidine (7.00 g, 26.6 mmol), 2-chloro-N-(4-mercapto-phenyl)-benzamide (6.33 g, 27.9 mmol) and acetonitrile (100 mL) under nitrogen. Once the solid had dissolved, the reaction mixture was cooled to 0° C. and triethylamine (3.7 mL, 26.6 mmol) was added dropwise. The solution was stirred at 0° C. for 10 min and then allowed to warm to room temperature and stirred for 1 h. After this time, water (50 mL) was added and a white solid precipitated and the reaction mixture stirred for an additional 4 h. After this time, the reaction mixture was filtered and the solid washed with acetonitrile (2×10 mL) to give the title compound as a white solid (8.03 g, 74%). 1H NMR (DMSO) 7.4-7.6 (5H, m), 7.7 (1H, s), 7.80-7.85 (2H, d), 10.9 (1H, s). MS (ES+): 412

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07767672B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-3fc13ab3e31147429fd8e9a10807efd1
출처 메모uspto-grants-2010_08