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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203341Generated: October 31, 2026

Phosphorus oxychloride → 6-Chloro-3-(3,3,4,4,4-pentafluorobutyl)imidazo[1,5-a]pyridine

https://huagongshe.com/reaction/2203341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantN-[(5-chloropyridin-2-yl)methyl]-4,4,5,5,5-pentafluoropentanamideHCID 86678976—
Solvent1,2-DichloroethaneHCID 11—
Product6-Chloro-3-(3,3,4,4,4-pentafluorobutyl)imidazo[1,5-a]pyridineHCID 86678977—

Reaction Steps

To a solution of the intermediate from Step F (7.1 g, 22.42 mmol) in 1,2-dichloroethane (30 mL) was added phosphorous oxychloride (10.45 mL, 112 mmol). The resulting mixture was refluxed for 18 hours. The reaction mixture was cooled to room temperature and concentrated. The residue was partitioned between water and ethyl acetate. The aqueous layer was neutralized with solid sodium bicarbonate and then extracted with ethyl acetate (3×). The organic layer was washed with brine, dried over anhydrous sodium sulfate, filtered, and concentrated. The residue was purified by silica gel chromatography using a hexanes/EtOAc gradient to give a light yellow solid. m/z=298.9 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365574B2
Source datasetuspto-grants-2016_06
ORD IDord-b97cc0b68b9c43ed8b57d97fd0bd4b12
Source noteuspto-grants-2016_06