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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 450380생성일: 2026년 10월 25일

Diisopropylethylamine → N2-[(1S)-1-(5-Fluoropyrimidin-2-yl)ethyl]-N4-(5-isopropoxy-1H-pyrazol-3-yl)-5-nitropyrimidine-2,4-diamine

https://huagongshe.com/reaction/450380

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참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물(S)-1-(5-Fluoropyrimidin-2-yl)ethanamine hydrochlorideHCID 66624037—
반응물HCID 178458615HCID 178458615—
용매1-ButanolHCID 263—
용매Ethyl AcetateHCID 8857—
생성물N2-[(1S)-1-(5-Fluoropyrimidin-2-yl)ethyl]-N4-(5-isopropoxy-1H-pyrazol-3-yl)-5-nitropyrimidine-2,4-diamineHCID 17845866374%

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온도70 °C

반응 단계

A mixture of 2-chloro-N-(5-isopropoxy-1H-pyrazol-3-yl)-5-nitropyrimidin-4-amine (Intermediate 30, 0.2 g) and [(1S)-1-(5-fluoropyrimidin-2-yl)ethyl]amine hydrochloride (Intermediate 15, 0.15 g) in n-BuOH (5 mL) with diisopropylethylamine (1 mL) was stirred at 70° C. for 4 hours. The resulting mixture was diluted with ethyl acetate (20 mL), and washed with brine (10 mL×3). The organic layer was dried and concentrated. The resulting residue was separated by silica gel column (Hexane/Ethyl acetate) to yield 0.2 g of title compound. MS (electrospray): 404 (M+1) for C16H18FN9O3.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08486966B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-56b663976e9048a18946e34c79d06c3a
출처 메모uspto-grants-2013_07