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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 245847Generated: October 31, 2026

Phosphorus oxychloride → 6-Fluoroimidazo[1,5-A]pyridine

https://huagongshe.com/reaction/245847

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantN-[(5-Fluoro-2-pyridinyl)methyl]formamideHCID 86677902—
SolventTolueneHCID 1140—
Product6-Fluoroimidazo[1,5-A]pyridineHCID 7174400396%

Reaction Conditions

Temperature100 °C

Reaction Steps

In a round-bottomed flask, N-(5-fluoro-pyridin-2-ylmethyl)-formamide (612 mg, 3.97 mmol) was dissolved in toluene (16 ml) and phosphorus oxychloride (0.68 ml, 7.3 mmol) was added. The reaction mixture was stirred at 100° C. in an oil bath for 4 h then cooled to 0° C. and carefully quenched with ice. Aqueous 25% ammonium hydroxide was added until pH=˜9. The mixture was diluted with water and extracted with dichloromethane (3×). The organic layers were combined, dried over sodium sulfate, filtered and concentrated to give 517 mg (96%) of 6-fluoro-imidazo[1,5-a]pyridine as a light brown oil. 1H NMR (CDCl3, 300 MHz): δ (ppm) 8.16 (s, 1H), 7.84-7.94 (m, 1H), 7.50 (s, 1H), 7.46 (dd, J=9.8, 5.3 Hz, 1H), 6.69 (ddd, J=9.8, 7.7, 2.1 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658646B2
Source datasetuspto-grants-2014_02
ORD IDord-c3a2821918b145de94ff4b42882b74b3
Source noteuspto-grants-2014_02