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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2171872생성일: 2026년 10월 26일

Acetic Acid → HCID 178442411, 화합물

https://huagongshe.com/reaction/2171872

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 번호US09051319B2
출처 데이터셋uspto-grants-2015_06
ORD IDord-8529576a69794fbbb74459923dc1bf04
출처 메모uspto-grants-2015_06