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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2102319Generated: October 26, 2026

Sodium Hydroxide → 3-(beta-d-Glucopyranosyloxy)-4-[(4-methylthiophenyl)methyl]-1h-pyrazole

https://huagongshe.com/reaction/2102319

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactantalpha-D-Glucopyranosyl bromide, tetraacetateHCID 101776—
Reactant4-[(4-Methylthiophenyl)methyl]-5-phenyl-1,2-dihydro-3h-pyrazole-3-oneHCID 66971062—
CatalystBenzenemethanaminium, N,N,N-tributyl-, bromideHCID 2724282—
SolventDichloromethaneHCID 6344—
Product3-(beta-d-Glucopyranosyloxy)-4-[(4-methylthiophenyl)methyl]-1h-pyrazoleHCID 17850314629.4%

Reaction Steps

To a suspension of 4-[(4-methylthiophenyl)methyl]-5-phenyl-1,2-dihydro-3H-pyrazole-3-one (0.087 g), acetobromo-α-D-glucose (0.62 g) and benzyltri(n-butyl)ammonium bromide (0.054 g) in dichloromethane (3 mL) was added a sodium hydroxide aqueous solution (5 mol/L, 0.9 mL), and the mixture was stirred at room temperature overnight. The reaction mixture was purified by column chromatography on aminopropylated silica gel (eluent: tetrahydrofuran). The obtained semi purified 4-[(4-methylthiophenyl)methyl]-3-(2,3,4,6-tetraacethyl-β-D-glucopyranosyloxy)-1H-pyrazole was dissolved in methanol (5 mL), and sodium methoxide (28% methanol solution, 0.28 mL) was added to the solution. The mixture was stirred at room temperature for 2 hours. Acetic acid (0.090 g) was added to the reaction mixture, and the solvent was removed. Water (5 mL) was added to the residue, and the mixture was purified by solid phase extraction on ODS (washing solvent: water/methanol=5/1, eluent: methanol). Column chromatography on silica gel (eluent: dichloromethane/methanol=20/1-7/1) was used for further purification to give the title compound (0.033 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576063B2
Source datasetuspto-grants-2009_08
ORD IDord-123539307f5a47ba9d770d4f37f6024a
Source noteuspto-grants-2009_08