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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2189866생성일: 2026년 10월 26일

Methylamine → (S)-6-(5-Cyclopropyl-1H-pyrazol-3-ylamino)-5-fluoro-2-(1-(4-fluorophenyl)ethylamino)-4-(methylamino)nicotinonitrile

https://huagongshe.com/reaction/2189866

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참여 물질

역할이름HCID투입량
반응물MethylamineHCID 6329—
반응물DichloromethaneHCID 6344—
반응물DiisopropylethylamineHCID 81531—
반응물(S)-6-(5-cyclopropyl-1H-pyrazol-3-ylamino)-5-fluoro-2-(1-(4-fluorophenyl)ethylamino)-4-iodonicotinonitrileHCID 67456774—
용매1-ButanolHCID 263—
생성물(S)-6-(5-Cyclopropyl-1H-pyrazol-3-ylamino)-5-fluoro-2-(1-(4-fluorophenyl)ethylamino)-4-(methylamino)nicotinonitrileHCID 1154600951.4%

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온도185 °C

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To a solution of (S)-6-(5-cyclopropyl-1H-pyrazol-3-ylamino)-5-fluoro-2-(1-(4-fluorophenyl)ethylamino)-4-iodonicotinonitrile (Example 134, 0.10 g, 0.19 mmol) and DIEA (0.03 g, 0.25 mol) in n-BuOH (1.5 ml) was added methylamine (2.0 M in THF, 1.9 mmol). The reaction was then heated to 185° C. under microwave conditions (1 hour×2 cycles). The reaction was then cooled to room temperature, DCM (10 ml) was added, and washed with 10% aqueous Na2S2O3. The organic layer was then dried over Na2SO4, filtered, and then concentrated. The resulting oil was purified by reverse-phase column chromatography (5-50% ACN) to give the title compound (0.04 g, 49%). 1H NMR (400 MHz, CD3OD) δ 7.35 (br s, 2H), 7.04-7.00 (m, 2H), 5.95 (br s, 1H), 5.14 (br s, 1H), 3.15 (d, J=2.7 Hz, 3H), 1.87-1.82 (m, 1H), 1.52 (d, J=6.8 Hz, 3H), 0.95-0.94 (m, 2H), 0.65-0.63 (m, 2H). MS: Calcd.: 409; Found: [M+H]+ 410.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08324252B2
출처 데이터셋uspto-grants-2012_12
ORD IDord-30dc814d006f45c0a02d3ffd35880fc8
출처 메모uspto-grants-2012_12