HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910589Generated: October 29, 2026
Potassium Carbonate → 1-acetyl-4-[(4-isopropoxyphenyl)-methyl]-5-methyl-3-(2,3,4,6-tetra-O-pivaloyl-beta-D-glucopyranosyloxy)-1H-pyrazole
https://huagongshe.com/reaction/910589
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | ((2R,3R,4S,5R,6R)-6-bromo-3,4,5-tris(2,2-dimethylpropanoyloxy)oxan-2-yl)methyl 2,2-dimethylpropanoate | HCID 10886360 | — |
| Reactant | 1-acetyl-5-methyl-4-{[4-(propan-2-yloxy)phenyl]methyl}-2,3-dihydro-1H-pyrazol-3-one | HCID 67349636 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-acetyl-4-[(4-isopropoxyphenyl)-methyl]-5-methyl-3-(2,3,4,6-tetra-O-pivaloyl-beta-D-glucopyranosyloxy)-1H-pyrazole | HCID 67349863 | 80.2% |
Reaction Steps
To a suspension of 1-acetyl-1,2-dihydro-4-[(4-isopropoxyphenyl)methyl]-5-methyl-3H-pyrazol-3-one (1.00 g) in acetonitrile (5 mL) and tetrahydrofuran (3 mL) was added potassium carbonate (0.719 g) under stirring at room temperature. After stirring the mixture at 50° C. for 1 hour, 2,3,4,6-tetra-O-pivaloyl-α-D-glucopyranosyl bromide (2.35 g) was added to the mixture. The mixture was stirred at 50° C. for 12 hours. After the reaction completed, the insoluble materials were removed by filtration, and the filtrate was concentrated under reduced pressure. 2-Propanol was added to the residue, and the mixture was re-concentrated under reduced pressure. The residue was recrystallized in the mixed solvent of water and methanol, the obtained crystals were dried under reduced pressure to give 1-acetyl-4-[(4-isopropoxyphenyl)methyl]-5-methyl-3-(2,3,4,6-tetra-O-pivaloyl-β-D-glucopyranosyloxy)-1H-pyrazole (2.19 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08022192B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-b6aa6092894b4acdaa8f85311657e243 |
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| Source note | uspto-grants-2011_09 |
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