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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 77709생성일: 2026년 10월 24일

3-(Trifluoromethyl)phenyl isocyanate → N-[4-Methyl-3-(9H-pyrimido[4,5-b]indol-6-yl)phenyl]-N'-[3-(trifluoromethyl)-phenyl]urea

https://huagongshe.com/ko/reaction/77709

반응식

참여 물질

역할이름HCID투입량
반응물3-(Trifluoromethyl)phenyl isocyanateHCID 9483—
반응물DiisopropylethylamineHCID 81531—
반응물4-methyl-3-(9H-pyrimido[4,5-b]indol-6-yl)anilineHCID 69043120—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
생성물N-[4-Methyl-3-(9H-pyrimido[4,5-b]indol-6-yl)phenyl]-N'-[3-(trifluoromethyl)-phenyl]ureaHCID 59774725—

반응 단계

To 1-isocyanato-3-(trifluoromethyl)benzene (9.8 μl, 0.070 mmol) was added a solution of 4-methyl-3-(9H-pyrimido[4,5-b]indol-6-yl)aniline (17.5 mg, 0.064 mmol) and DIPEA (16 μL, 0.089 mmol) in THF (0.4 mL). The reaction was stirred at ambient temperature until LCMS indicated complete reaction, typically 16 hours. The reaction mixture was diluted to a total of 2 mL with THF and MeOH and purified by preparative LCMS to recover the product as a TFA salt (17.1 mg, 46.6%). 1H NMR (300 MHz, DMSO): δ 13.1 (bs, 1H), 9.66 (s, 1H), 9.15 (s, 2H), 8.92 (s, 1H), 8.33 (s, 1H), 8.01 (s, 1H), 7.72 (d, 1H), 7.62 (dd, 1H), 7.4-7.6 (m, 3H), 7.2-7.4 (m, 3H), 2.21 (s, 3H). MS (EI) m/z=462 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841318B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-c38b2953652d47b685573ba2f8d9f2d5
출처 메모uspto-grants-2014_09