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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910597Generated: October 29, 2026

Water → 4-benzyl-5-isopropyl-3-(2,3,4,6-tetra-O-pivaloyl-betaD-glucopyranosyloxy)-1H-pyrazole

https://huagongshe.com/reaction/910597

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium BicarbonateHCID 516892—
Reactant4-benzyl-1-ethoxycarbonyl-5-isopropyl-3-(2,3,4,6-tetra-O-pivaloyl-beta-D-glucopyranosyl-oxy)-1H-pyrazoleHCID 67350610—
SolventMethanolHCID 887—
Product4-benzyl-5-isopropyl-3-(2,3,4,6-tetra-O-pivaloyl-betaD-glucopyranosyloxy)-1H-pyrazoleHCID 6734948471.9%

Reaction Steps

To a solution of 4-benzyl-1-ethoxycarbonyl-5-isopropyl-3-(2,3,4,6-tetra-O-pivaloyl-β-D-glucopyranosyl-oxy)-1H-pyrazole (0.15 g) in methanol (3 mL) was added sodium bicarbonate (0.032 g) under stirring at room temperature. The mixture was stirred at room temperature for 12 hours. In addition, to the mixture was added potassium carbonate (0.053 g), and the mixture was stirred for 2 hours. The reaction mixture was poured into water to precipitate the solid. The solids were collected by filtration. The obtained solids were washed with water and dried under reduced pressure to give 4-benzyl-5-isopropyl-3-(2,3,4,6-tetra-O-pivaloyl-β-D-glucopyranosyloxy)-1H-pyrazole (0.098 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022192B2
Source datasetuspto-grants-2011_09
ORD IDord-81865059d8eb4ca181d4e598609cb91b
Source noteuspto-grants-2011_09