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HRID 7384作成日:2026年10月24日

Cesium carbonate → 3-(beta-D-glucopyranosyloxy)-1-(2-hydroxyethyl)-5-methyl-4-[(4-cyclopropylphenyl)methyl]-1H-pyrazole

https://huagongshe.com/ja/reaction/7384

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物1-Acetoxy-2-bromoethaneHCID 13564—
反応物Sodium HydroxideHCID 14798—
反応物3-(beta-D-glucopyranosyloxy)-5-methyl-4-[(4-cyclopropylphenyl)methyl]-1H-pyrazoleHCID 69013246—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物3-(beta-D-glucopyranosyloxy)-1-(2-hydroxyethyl)-5-methyl-4-[(4-cyclopropylphenyl)methyl]-1H-pyrazoleHCID 69134461—

反応手順

To a suspension of 3-(β-D-glucopyranosyloxy)-5-methyl-4-[(4-cyclopropylphenyl)methyl]-1H-pyrazole (33 mg) and cesium carbonate (138 mg) in N,N-dimethylformamide (1 mL) was added 2-bromoethyl acetate (0.035 mL) at 40° C., and the mixture was stirred for 2 hours. To the reaction mixture was added water, and the mixture was purified by solid phase extraction on ODS (washing solvent: distilled water, eluent: methanol). The obtained crude product was dissolved in methanol (1 mL), and to the solution was added 2 mol/L aqueous sodium hydroxide solution (0.04 mL), and the mixture was stirred at room temperature for 30 minutes. The solvent was removed under reduced pressure, and the residue was purified by column chromatography on ODS (developing solvent: methanol/water=3/2) to give 3-(β-D-glucopyranosyloxy)-1-(2-hydroxyethyl)-5-methyl-4-[(4-cyclopropylphenyl)methyl]-1H-pyrazole (8 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087579B2
出典データセットuspto-grants-2006_08
ORD IDord-e1891c54274e463798b044aadeb68576
出典メモuspto-grants-2006_08