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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6657생성일: 2026년 10월 25일

Water → 1-(benzyloxy-carbonyl)-3-(6-O-ethoxycarbonyl-beta-D-glucopyranosyloxy)-4-((4-isopropoxyphenyl)methyl]-5-methylpyrazole

https://huagongshe.com/reaction/6657

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Ethyl chloroformateHCID 10928—
반응물2-Hydroxy-1,2,3-propanetricarboxylic acid hydrate (1:1)HCID 22230—
반응물1-(benzyloxycarbonyl)-3-(beta-D-gluco-pyranosyloxy)-4-[(4-isopropoxyphenyl)methyl]-5-methyl-pyrazoleHCID 67334988—
용매2,4,6-TrimethylpyridineHCID 7953—
생성물1-(benzyloxy-carbonyl)-3-(6-O-ethoxycarbonyl-beta-D-glucopyranosyloxy)-4-((4-isopropoxyphenyl)methyl]-5-methylpyrazoleHCID 23543164—

반응 단계

To a solution of 1-(benzyloxycarbonyl)-3-(β-D-glucopyranosyloxy)-4-[(4-isopropoxyphenyl)methyl]-5-methylpyrazole (0.20 g) in 2,4,6-trimethylpyridine (4 mL) was added ethyl chloroformate (0.092 mL), and the mixture was stirred at room temperature for 1 day. To the reaction mixture were added water and citric acid monohydrate, and the resulting mixture was extracted with ethyl acetate. The organic layer was washed with water, 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) to give 1-(benzyloxycarbonyl)-3-(6-O-ethoxycarbonyl-β-D-glucopyranosyloxy)-4-[(4-isopropoxyphenyl)methyl]-5-methylpyrazole (0.17 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07084123B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-98f3503a6a674d06900034c5fded6da5
출처 메모uspto-grants-2006_08