HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → (6-Fluoro-1-iodo-imidazo[1,5-a]pyridin-3-yl)-methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (6-Fluoro-imidazo[1,5-a]pyridin-3-yl)-methanol | HCID 86677906 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | (6-Fluoro-1-iodo-imidazo[1,5-a]pyridin-3-yl)-methanol | HCID 71280570 | 50% |
Reaction Steps
In a round-bottomed flask, (6-fluoro-imidazo[1,5-a]pyridin-3-yl)-methanol (225 mg, 1.15 mmol) was dissolved in ethanol (2 ml) and water (1 ml). Sodium bicarbonate (341 mg, 4.06 mmol) was added followed by iodine (383 mg, 1.51 mmol). The dark brown suspension was stirred at room temperature for 3 h then quenched with 10% Na2S2O3-solution and extracted with EtOAc (2×). The organic layers were washed with water and brine then dried over sodium sulfate, filtered and concentrated. The residue was absorbed on silica gel and chromatographed with EtOAc/hexanes (gradient 0-40% EtOAc) to provide 157 mg (50%, 2 steps) of (6-fluoro-1-iodo-imidazo[1,5-a]pyridin-3-yl)-methanol as a light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08658646B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-7ec3c0ae825d4f8b96b650a10b4c9233 |
| Source note | uspto-grants-2014_02 |