HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → 2-fluoro-5-(4-(iodomethyl)tetrahydro-2H-pyran-4-yl)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | (4-(6-fluoropyridin-3-yl)tetrahydro-2H-pyran-4-yl)methanol | HCID 118045465 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-fluoro-5-(4-(iodomethyl)tetrahydro-2H-pyran-4-yl)pyridine | HCID 118045224 | 60.6% |
Reaction Steps
To an ice cooled solution of triphenylphosphine (983 mg, 3.75 mmol), iodine (952 mg, 3.75 mmol) in dichloromethane (20 mL) was added imidazole (278 mg, 4.09 mmol). The solution was stirred at ambient temperature for 1 h, followed by the addition of (4-(6-fluoropyridin-3-yl)tetrahydro-2H-pyran-4-yl)methanol (360 mg, 1.70 mmol) in 10 mL dichloromethane. The reaction mixture was heated to 60° C. in an oil bath for 48 h. Solid was filtered off, the filtrate was purified by flash column chromatography on silicagel (ISCO) eluting with 0-80% ethyl acetate in heptane to give to give 2-fluoro-5-(4-(iodomethyl)tetrahydro-2H-pyran-4-yl)pyridine (330 mg, 1.03 mmol, 60.3% yield) as light yellow color oil. LCMS (m/z): 322 (MH+), 0.77 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09242996B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-e518d87dac2c480bbca8c40730fb90c5 |
| Source note | uspto-grants-2016_01 |