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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488344Generated: November 1, 2026

alpha-D-Glucopyranosyl bromide, tetraacetate → 4-[(4-Isopropoxy-phenyl)methyl]-5-methyl-3-(2,3,4,6-tetra-o-acetyl-beta-d-glucopyranosyloxy)-1h-pyrazole

https://huagongshe.com/reaction/488344

Reaction equation

Participants

RoleNameHCIDCharge
Reactantalpha-D-Glucopyranosyl bromide, tetraacetateHCID 101776—
Reactant4-(4-Isopropoxybenzyl)-5-methyl-1H-pyrazol-3(2H)-oneHCID 15542324—
CatalystHCID 178418647HCID 178418647—
SolventTetrahydrofuranHCID 8028—
Product4-[(4-Isopropoxy-phenyl)methyl]-5-methyl-3-(2,3,4,6-tetra-o-acetyl-beta-d-glucopyranosyloxy)-1h-pyrazoleHCID 6733507739%

Reaction Steps

To a suspension of 1,2-dihydro-4-[(4-isopropoxy-phenyl)methyl]-5-methyl-3H-pyrazol-3-one (46 mg), acetobromo-α-D-glucose (99 mg) and 4A molecular sieves in tetrahydrofuran (3 mL) was added silver carbonate (66 mg), and the mixture was stirred under shading the light at 65° C. overnight. The reaction mixture was purified by column chromatography on aminopropyl silica gel (eluent:tetrahydrofuran). Further purification by preparative thin layer chromatography on silica gel (developing solvent:ethyl acetate/hexane=2/1) afforded 4-[(4-isopropoxyphenyl)methyl]-5-methyl-3-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy)-1H-pyrazole (42 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06972283B2
Source datasetuspto-grants-2005_12
ORD IDord-bb0ba203304c445ca09b0fb4513d3148
Source noteuspto-grants-2005_12