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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1351108생성일: 2026년 10월 25일

Water → HCID 69516928, 화합물

https://huagongshe.com/reaction/1351108

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium CarbonateHCID 11430—
반응물3-(Bromomethyl)phenyl acetateHCID 6422075—
반응물3-(beta-D-glucopyranosyloxy)-4-(2-hydroxybenzyl)-5-isopropyl-1H-pyrazoleHCID 69516549—
용매DimethylformamideHCID 6228—
생성물HCID 69516928HCID 69516928—

반응 단계

To a solution of 3-(β-D-glucopyranosyloxy)-4-(2-hydroxybenzyl)-5-isopropyl-1H-pyrazole (150 mg) in N,N-dimethylformamide (1 mL) were added 3-bromomethylphenyl acetate (131 mg) and potassium carbonate (105 mg), and the mixture was stirred at room temperature for 13 hours. The reaction mixture was poured into water, and the resulting mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue was purified by column chromatography on silica gel (eluent: dichloromethane/methanol=10/1˜5/1) to give 4-[2-(3-acetyloxybenzyloxy)benzyl]-3-(β-D-glucopyranosyloxy)-5-isopropyl-1H-pyrazole. To a solution of 4-[2-(3-acetyloxybenzyloxy)benzyl]-3-(β-D-glucopyranosyloxy)-5-isopropyl-1H-pyrazole (12 mg) in methanol (2 mL) was added sodium methoxide (28% methanol solution, 5 μL), and the mixture was stirred at room temperature for 1 hour. The reaction mixture was concentrated under reduced pressure, and the residue was purified by solid phase extraction on ODS (washing solvent: distilled water, eluent: methanol) to give the title compound (8 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07217697B2
출처 데이터셋uspto-grants-2007_05
ORD IDord-6fcedb9fb67042d9882f3a921a9a145d
출처 메모uspto-grants-2007_05