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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 540495생성일: 2026년 10월 23일

2-Naphthyl isocyanate → 1-[3-(4-Bromo-2-methyl-2H-pyrazol-3-yl)-4-methoxy-phenyl]-3-naphthalen-2-yl-urea

https://huagongshe.com/ko/reaction/540495

반응식

참여 물질

역할이름HCID투입량
반응물2-Naphthyl isocyanateHCID 16718—
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-naphthalen-2-yl-ureaHCID 1177530675%

반응 단계

3-(4-Bromo-2-methyl-2H-pyrazol-3-yl)-4-methoxy-phenylamine (0.035 g, 0.12 mmol) was treated with 2-naphthyl isocyanate (0.023 g, 0.13 mmol, 1.05 equiv.) in CH2Cl2 (1 mL), in a similar manner as described in Example 1.2 to afford Compound 14 (0.040 g, 0.09 mmol, 70%) as a white solid. LCMS m/z (%)=451 (M+H79Br, 95), 453 (M+H81Br, 100). 1H NMR (400 MHz, acetone-d6) δ: 8.30 (s, 1H), 8.20 (s, 1H), 8.19 (d, J=1.8 Hz, 1H), 7.56-7.84 (m, 3H), 7.72 (dd, J=2.7, 9.0 Hz, 1H), 7.56 (dd, J=2.1, 8.8 Hz, 1H), 7.50 (s, 1H), 7.48 (d, J=2.7 Hz, 1H), 7.44 (t, J=8.0 Hz, 1H), 7.14 (t, J=8.0 Hz, 1H), 3.83 (s, 3H), 3.70 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08871797B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-3d44bbb6d37f454d8f393ae34de29ccf
출처 메모uspto-grants-2014_10