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HRID 7397作成日:2026年10月24日

Water → 1-(cyclopropylmethyl)-3-(6-O-ethoxycarbonyl-beta-D-glucopyranosyloxy)-4-[(4-isopropoxyphenyl)methyl]-5-methyl-1H-pyrazole

https://huagongshe.com/ja/reaction/7397

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-(cyclopropylmethyl)-3-(beta-D-glucopyranosyloxy)-4-[(4-isopropoxyphenyl)methyl]-5-methyl-1H-pyrazoleHCID 69133847—
溶媒2,4,6-TrimethylpyridineHCID 7953—
生成物1-(cyclopropylmethyl)-3-(6-O-ethoxycarbonyl-beta-D-glucopyranosyloxy)-4-[(4-isopropoxyphenyl)methyl]-5-methyl-1H-pyrazoleHCID 2354551374.4%

反応手順

To a solution of 1-(cyclopropylmethyl)-3-(β-D-glucopyranosyloxy)-4-[(4-isopropoxyphenyl)methyl]-5-methyl-1H-pyrazole (0.050 g) in 2,4,6-trimethylpyridine (1 mL) was added ethyl chloroformate (0.035 g), and the mixture was stirred at room temperature overnight. Citric acid monohydrate (3.3 g) and water were added to the reaction mixture, and the mixture was purified by solid phase extraction on ODS (washing solvent: distilled water, eluent: methanol), and successively by column chromatography on silica gel (eluent: dichloromethane/methanol=10/1) to give 1-(cyclopropylmethyl)-3-(6-O-ethoxycarbonyl-β-D-glucopyranosyloxy)-4-[(4-isopropoxyphenyl)methyl ]-5-methyl-1H-pyrazole (0.043 g).

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-a263acd080c74398b09f94a2fc949eda
出典メモuspto-grants-2006_08