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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 75908생성일: 2026년 10월 24일

Diisopropylethylamine → AZ-960

https://huagongshe.com/ko/reaction/75908

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참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물(S)-1-(4-Fluorophenyl)-ethylamineHCID 2779063—
반응물(S)-5-Chloro-N6-(5-cyclopropyl-1H-pyrazol-3-yl)-N2-(1-(4-fluorophenyl)ethyl)pyridine-2,3,6-triamineHCID 68522447—
용매1-ButanolHCID 263—
용매WaterHCID 962—
생성물AZ-960HCID 2509918491%

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온도130 °C

반응 단계

A suspension of 2,5-difluoro-6-(5-methyl-1H-pyrazol-3-ylamino)nicotinonitrile (Method 41, 0.20 g, 0.85 mmol), DIEA (0.14 g, 1.1 mmol), and (S)-1-(4-fluorophenyl)ethanamine (0.23 g, 1.7 mmol) in n-BuOH (2 ml) was heated to 130° C. for 18 hours. The reaction was then cooled to room temperature, diluted with water (20 ml), and extracted with DCM (2×50 ml). 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 (0.27 g, 91%). 1H NMR (400 MHz, CD3OD) δ 7.38-7.32 (m, 3H), 7.03-6.99 (m, 2H), 5.99 (br s, 1H), 5.15-5.14 (m, 1H), 2.24 (s, 3H), 1.53 (d, J=6.8 Hz, 3H). MS: Calcd.: 354. Found: [M+H]+ 355.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08835465B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-b8c9e5db3a2648b28c3e65b067b4bb83
출처 메모uspto-grants-2014_09