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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33132Generated: October 26, 2026

Water → 3-(6-O-ethoxy-carbonyl-beta-D-glucopyranosyloxy)-4-[(4-isopropoxyphenyl)-methyl]-1-isopropyl-5-methylpyrazole

https://huagongshe.com/reaction/33132

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl chloroformateHCID 10928—
Reactant2-Hydroxy-1,2,3-propanetricarboxylic acid hydrate (1:1)HCID 22230—
ReactantRemogliflozinHCID 9846588—
Solvent2,4,6-TrimethylpyridineHCID 7953—
Product3-(6-O-ethoxy-carbonyl-beta-D-glucopyranosyloxy)-4-[(4-isopropoxyphenyl)-methyl]-1-isopropyl-5-methylpyrazoleHCID 8660278972.7%

Reaction Steps

To a solution of 3-(β-D-glucopyranosyloxy)-4-[(4-iso-propoxyphenyl)methyl]-1-isopropyl-5-methylpyrazole (0.10 g) in 2,4,6-trimethylpyridine (1 mL) was added ethyl chloroformate (0.072 g), and the mixture was stirred at room temperature overnight. To the reaction mixture were added citric acid monohydrate (3.3 g) and water, and the resulting mixture was purified by ODS solid phase extraction (washing solvent: distilled water, eluent: methanol). Further purification by column chromatography on silica gel (eluent: dichloromethane/methanol=10/1) and recrystallization (recrystallization solvent: ethyl acetate/hexane=1/3) afforded 3-(6-O-ethoxy-carbonyl-β-D-glucopyranosyloxy)-4-[(4-isopropoxyphenyl)methyl]-1-isopropyl-5-methylpyrazole (0.084 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429568B2
Source datasetuspto-grants-2008_09
ORD IDord-4f889f2c3e8f4a7fbe3c8ca1366ea54d
Source noteuspto-grants-2008_09