HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2088989Generated: October 25, 2026
Diisopropylethylamine → 2-Chloro-6-(3,3-difluoroazetidin-1-yl)-4-iodopyridine
https://huagongshe.com/reaction/2088989
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3,3-Difluoroazetidine hydrochloride | HCID 2758247 | — |
| Reactant | 2,6-Dichloro-4-iodopyridine | HCID 11737393 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Chloro-6-(3,3-difluoroazetidin-1-yl)-4-iodopyridine | HCID 86649868 | 49.7% |
Reaction Steps
To a suspension of 2,6-dichloro-4-iodopyridine (1 g, 3.65 mmol) and 3,3-difluoroazetidine hydrochloric acid salt (0.497 g, 3.83 mmol) in 25 mL tetrahydrofuran was added diisopropylethylamine (0.797 ml, 4.56 mmol). The reaction mixture was heated at 90° C. for 16 hours. Further addition of another equivalent of amine and base was performed, and the suspension was heated at 100° C. for several hours, and then cooled, diluted with ethyl acetate, washed with water, brine, dried over MgSO4, filtered, and concentrated. The residue was purified on silica gel using flash chromatography (5% to 20% ethyl acetate/hexane) to afford 0.6 g of the title compound. MS (DCI+) m/z 331.0 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08435980B2 |
|---|
| Source dataset | uspto-grants-2013_05 |
|---|
| ORD ID | ord-04b73413fc8f47f59614d0371babcbdc |
|---|
| Source note | uspto-grants-2013_05 |
|---|