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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | 2-(Biphenyl-4-ylmethyl)-7-isobutyl-5-methyl-2h-pyrazolo[3,4-d]pyrimidine-4,6(5h,7h)-dione | HCID 68505460 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(biphenyl-4-ylmethyl)-3-iodo-7-isobutyl-5-methyl-2H-pyrazolo[3,4-d]pyrimidine-4,6(5H,7H)-dione | HCID 68505064 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08846693B2 |
|---|
| Source dataset | uspto-grants-2014_09 |
|---|
| ORD ID | ord-015f38ef5d244268a62e8df886a6a395 |
|---|
| Source note | uspto-grants-2014_09 |
|---|