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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81412Generated: October 26, 2026

Iodine → 2-(biphenyl-4-ylmethyl)-3-iodo-7-isobutyl-5-methyl-2H-pyrazolo[3,4-d]pyrimidine-4,6(5H,7H)-dione

https://huagongshe.com/reaction/81412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantLithium diisopropylamideHCID 2724682—
Reactant2-(Biphenyl-4-ylmethyl)-7-isobutyl-5-methyl-2h-pyrazolo[3,4-d]pyrimidine-4,6(5h,7h)-dioneHCID 68505460—
SolventTetrahydrofuranHCID 8028—
Product2-(biphenyl-4-ylmethyl)-3-iodo-7-isobutyl-5-methyl-2H-pyrazolo[3,4-d]pyrimidine-4,6(5H,7H)-dioneHCID 68505064—

Reaction Conditions

Temperature-78 °C

Reaction Steps

2-(biphenyl-4-ylmethyl)-7-isobutyl-5-methyl-2H-pyrazolo[3,4-d]pyrimidine-4,6(5H,7H)-dione (203 mg, 0.523 mmol) is dissolved in anhydrous THF (5 mL), and then cooled to −78° C. 1.8 M solution of LDA in THF (600 uL) is added dropwise with rigorous stirring at −78° C., followed by the addition of iodine (160 mg, 0.63 mmol) in THF. The reaction mixture is stirred at −78° C. for an hour, and then is allowed to warm up to room temperature before quenching. The mixture is poured into saturated NH4Cl solution, and then extracted with ethyl acetate three times. The combined organic phase is washed with potassium iodide aqueous solution (1 M), water, and then dried over Na2SO4. Solvent is removed under reduced vacuum to give crude product was white solids. MS (ESI) m/z 515.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846693B2
Source datasetuspto-grants-2014_09
ORD IDord-015f38ef5d244268a62e8df886a6a395
Source noteuspto-grants-2014_09