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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2375199생성일: 2026년 10월 26일

Citric Acid → 1-ethoxycarbonyl-3-(6-O-ethoxycarbonyl-beta-D-glucopyranosyl-oxy)-4-[(4-ethylthiophenyl)methyl]-5-methylpyrazole

https://huagongshe.com/reaction/2375199

반응식

참여 물질

역할이름HCID투입량
반응물Citric AcidHCID 311—
반응물2,4,6-TrimethylpyridineHCID 7953—
반응물Ethyl chloroformateHCID 10928—
반응물4-[(4-ethylthiophenyl)methyl]-3-(beta-D-glucopyranosyloxy)-5-methyl-1H-pyrazoleHCID 67337146—
생성물1-ethoxycarbonyl-3-(6-O-ethoxycarbonyl-beta-D-glucopyranosyl-oxy)-4-[(4-ethylthiophenyl)methyl]-5-methylpyrazoleHCID 23543166—

반응 단계

To a solution of 4-[(4-ethylthiophenyl)methyl]-3-(β-D-glucopyranosyloxy)-5-methyl-1H-pyrazole (0.03 g) in 2,4,6-trimethylpyridine (0.5 mL) was added ethyl chloroformate (0.021 mL), and the mixture was stirred at room temperature overnight. To the reaction mixture was added 10% aqueous citric acid solution, and the resulting mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue was purified by preparative thin layer chromatography on silica gel (eluent: dichloromethane/methanol=10/1) to give 1-ethoxycarbonyl-3-(6-O-ethoxycarbonyl-β-D-glucopyranosyloxy)-4-[(4-ethylthiophenyl)methyl]-5-methylpyrazole (0.023 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07465713B2
출처 데이터셋uspto-grants-2008_12
ORD IDord-eb397ad5e15b4ad5a4911929c4848862
출처 메모uspto-grants-2008_12