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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515935Generated: October 30, 2026

Imidazole → HCID 66802642, compound

https://huagongshe.com/reaction/515935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantIodineHCID 807—
ReactantTriphenylphosphineHCID 11776—
Reactant2'-Deoxy-2'-fluoro-2'-methyluridineHCID 11311503—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66802642HCID 6680264294%

Reaction Conditions

Temperature20 °C

Reaction Steps

Chiral 1-((2R,3R,4R,5R)-3-fluoro-4-hydroxy-5-hydroxymethyl-3-methyl-tetrahydro-furan-2-yl)-1H-pyrimidine-2,4-dione (6.14 g, 23.6 mmol), PPh3 (9 g, 34.4 mmol), imidazole (2.4 g, 34.4 mmol) and dry THF (100 mL) were added into a 3-neck flask bottle (500 mL), the mixture was stirred at 20° C. under nitrogen atmosphere for 20 min. Then I2 (6.6 g, 26 mmol) dissolved in dry THF (100 mL) was added into the mixture dropwise at 20° C. during 30 min, after addition, the whole mixture was stirred at 20° C. under nitrogen atmosphere for 18 hrs. TLC showed that the SM was consumed, then water (50 mL) was added into it, the mixture was extracted by EA (150 mL×3), organic layer was washed with brine, dried over Na2SO4, removed solvent by reduced pressure, residue was purified by silica gel chromatography column (DCM:MeOH=100:1 to 50:1) to afford the title compound as a white solid (8.2 g, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108999B2
Source datasetuspto-grants-2015_08
ORD IDord-3195089ff26a44eb95669b754bd2de8d
Source noteuspto-grants-2015_08