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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | N-[(5-Fluoro-2-pyridinyl)methyl]formamide | HCID 86677902 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 6-Fluoroimidazo[1,5-A]pyridine | HCID 71744003 | 96% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08658646B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-c3a2821918b145de94ff4b42882b74b3 |
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| Source note | uspto-grants-2014_02 |
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