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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1842819생성일: 2026년 10월 27일

Diisopropylethylamine → N-[4-(3-dimethylaminoazetidin-1-yl)-2-methoxy-5-nitrophenyl]-4-(1H-indol-3-yl)pyrimidin-2-amine

https://huagongshe.com/reaction/1842819

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참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물N,N-dimethylazetidin-3-amine dihydrochlorideHCID 22121220—
반응물N-(4-fluoro-2-methoxy-5-nitrophenyl)-4-(1H-indol-3-yl)pyrimidin-2-amineHCID 71240865—
용매DimethylacetamideHCID 31374—
생성물N-[4-(3-dimethylaminoazetidin-1-yl)-2-methoxy-5-nitrophenyl]-4-(1H-indol-3-yl)pyrimidin-2-amineHCID 7124081672.1%

반응 조건

온도140 °C

반응 단계

N,N-Dimethylazetidin-3-amine dihydrochloride (Intermediate 26, 140 mg, 0.81 mmol) was added to a suspension of N-(4-fluoro-2-methoxy-5-nitrophenyl)-4-(1H-indol-3-yl)pyrimidin-2-amine (Intermediate 68, 406 mg, 0.74 mmol) and DIPEA (0.514 mL, 2.94 mmol) in DMA (3 mL). The mixture was heated in a microwave at 140° C. for 0.5 h. The mixture was then part-purified by ion exchange chromatography, using an SCX column (20 g) and eluting with 0.35M methanolic ammonia. Appropriate fractions were combined nad concentrated in vacuo to provide an orange/brown gum. This gum was triturated with ethanol (15 mL) to give a solid which was collected by filtration and dried under vacuum to give the title compound (245 mg, 72%) as an orange solid; 1H NMR: 2.15 (6H, s), 3.17 (1H, dd), 3.76 (2H, dd), 3.97 (3H, s), 4.03-4.10 (2H, m), 6.29 (1H, s), 7.08 (1H, t), 7.14-7.21 (1H, m), 7.27 (1H, d), 7.45 (1H, d), 8.01 (1H, s), 8.28-8.37 (3H, m), 8.64 (1H, s), 11.79 (1H, s); m/z: ES+ MH+ 460.32.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08946235B2
출처 데이터셋uspto-grants-2015_02
ORD IDord-9af69b9920f04a7faee2a67e0fc708e5
출처 메모uspto-grants-2015_02