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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1055077생성일: 2026년 10월 24일

Acetic Acid → HCID 178442411, 화합물

https://huagongshe.com/ko/reaction/1055077

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물HydroxyureaHCID 3657—
반응물Sodium HydroxideHCID 14798—
반응물methyl 2,3-dibromo-5-((5-fluoro-2-(5-fluoro-1H-pyrrolo[2,3-b]pyridin-3-yl)pyrimidin-4-yl)amino)-6,6-dimethylheptanoateHCID 86714756—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물HCID 178442411HCID 178442411—

반응 단계

To a solution of NaOH (0.015 g) dissolved in water (0.410 mL) was added hydroxyurea (0.008 g, 0.100 mmol). The resulting mixture was stirred for 30 minutes before the dropwise addition of methyl 2,3-dibromo-5-((5-fluoro-2-(5-fluoro-1H-pyrrolo[2,3-b]pyridin-3-yl)pyrimidin-4-yl)amino)-6,6-dimethylheptanoate, 85a, (0.064 g, 0.110 mmol) in MeOH (0.150 mL). The solution was stirred for 6 hours before the addition of AcOH (0.031 mL). The residue was purified by reverse phase preparative HPLC to afford the desired product: 1H NMR (300 MHz, MeOD) δ 8.57 (dd, J=9.7, 2.8 Hz, 1H), 8.16 (d, J=5.5 Hz, 2H), 8.00 (d, J=4.1 Hz, 1H), 5.68 (s, 1H), 3.03 (ddd, J=27.4, 15.4, 12.3 Hz, 2H), 1.10 (d, J=3.3 Hz, 11H); LCMS Gradient 10-90%, 0.1% formic acid, 5 minutes, C18/ACN, RT=2.15 minutes (M+H) 416.04.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09394302B2
출처 데이터셋uspto-grants-2016_07
ORD IDord-1c44517c02f44aa592d5f8ced502462f
출처 메모uspto-grants-2016_07