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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 919393생성일: 2026년 10월 27일

Urea → 1-[3-(4-Bromo-2-methyl-2H-pyrazol-3-yl)-4-methoxy-phenyl]-3-(4-chloro-2-trifluoromethyl-phenyl)-urea

https://huagongshe.com/reaction/919393

반응식

참여 물질

역할이름HCID투입량
반응물UreaHCID 1176—
반응물4-Chloro-2-(trifluoromethyl)phenyl isocyanateHCID 2733264—
반응물3-(4-Bromo-1-methyl-1H-pyrazol-5-yl)-4-methoxyanilineHCID 11572741—
용매DichloromethaneHCID 6344—
생성물1-[3-(4-Bromo-2-methyl-2H-pyrazol-3-yl)-4-methoxy-phenyl]-3-(4-chloro-2-trifluoromethyl-phenyl)-ureaHCID 1128348460%

반응 단계

Urea synthesis (General Procedure): To a stirred solution of 3-(4-bromo-2-methyl-2H-pyrazol-3-yl)-4-methoxy-phenylamine (0.034 g, 0.12 mol, Example 1.1) in CH2Cl2 (1 mL) was added 4-chloro-2-(trifluoromethyl)phenyl isocyanate (0.029 g, 20.0 μL, 0.13 mmol, 1.05 equiv.) at room temperature. White solid precipitated and was filtered and washed with cold CH2Cl2 to afford Compound 9 (0.037 g, 0.074 mmol, 60%) as a white solid. LCMS m/z (%)=503 (M+H79Br, 77), 439 (M+H81Br, 100). 1H NMR (400 MHz, acetone-d6) δ: 8.82 (s, 1H), 8.22 (d, J=9.6 Hz, 1H), 7.62-7.72 (m, 4H), 7.49 (s, 1H), 7.43 (d, J=2.6 Hz, 1H), 7.15 (d, J=9.0 Hz, 1H), 3.83 (s, 3H), 3.68 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09273035B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-bbbc1c473e054251aeebbc78936b1c73
출처 메모uspto-grants-2016_03