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HRID 6657作成日:2026年10月26日

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

https://huagongshe.com/reaction/6657

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Ethyl chloroformateHCID 10928—
反応物2-Hydroxy-1,2,3-propanetricarboxylic acid hydrate (1:1)HCID 22230—
反応物1-(benzyloxycarbonyl)-3-(beta-D-gluco-pyranosyloxy)-4-[(4-isopropoxyphenyl)methyl]-5-methyl-pyrazoleHCID 67334988—
溶媒2,4,6-TrimethylpyridineHCID 7953—
生成物1-(benzyloxy-carbonyl)-3-(6-O-ethoxycarbonyl-beta-D-glucopyranosyloxy)-4-((4-isopropoxyphenyl)methyl]-5-methylpyrazoleHCID 23543164—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07084123B2
出典データセットuspto-grants-2006_08
ORD IDord-98f3503a6a674d06900034c5fded6da5
出典メモuspto-grants-2006_08