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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 75887생성일: 2026년 10월 25일

Diisopropylethylamine → (S)-N2-(5-Cyclopropyl-1H-pyrazol-3-yl)-3-fluoro-N6-(1-(4-fluorophenyl)ethyl)-5-nitropyridine-2,6-diamine

https://huagongshe.com/reaction/75887

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물3-cyclopropyl-1H-pyrazol-5-amineHCID 2758014—
반응물(S)-5,6-difluoro-N-(1-(4-fluorophenyl)ethyl)-3-nitropyridin-2-amineHCID 67452698—
용매TetrahydrofuranHCID 8028—
생성물(S)-N2-(5-Cyclopropyl-1H-pyrazol-3-yl)-3-fluoro-N6-(1-(4-fluorophenyl)ethyl)-5-nitropyridine-2,6-diamineHCID 6745402766.2%

반응 조건

온도55 °C

반응 단계

To a solution of (S)-5,6-difluoro-N-(1-(4-fluorophenyl)ethyl)-3-nitropyridin-2-amine (Method 23, 0.60 g, 2.0 mmol) in THF (10 ml) at room temperature was added 5-cyclopropyl-1H-pyrazol-3-amine (0.50 g, 4.0 mmol), and DIEA (0.26 g, 2.0 mmol). The reaction was then heated to 55° C. for 24 hours, cooled to room temperature, and quenched with water. The reaction was then extracted with DCM (2×75 ml), and the combined organic fractions were dried over Na2SO4, filtered, and then concentrated. The resulting oil was purified by column chromatography (DCM-MeOH=100:1) to give the title compound (0.53 g, 66%). 1H NMR (400 MHz, CD3OD) δ 8.00 (d, J=11.1 Hz, 1H), 7.38-7.35 (m, 2H), 7.07-7.02 (m, 2H), 6.17 (s, 1H), 5.41-5.39 (m, 1H), 1.93-1.87 (m, 1H), 1.61 (d, J=7.0 Hz, 3), 1.02-1.00 (m, 2H), 0.69-0.66 (m, 2H). MS: Calcd.: 400. Found: [M+H]+ 401.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08835465B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-9c2a28e7f4ea41ffaf0f6496383203e8
출처 메모uspto-grants-2014_09