HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221425Generated: October 31, 2026
Phosphorus oxide (P4O10) → 3-(Trifluoromethyl)imidazo[1,5-a]pyrazine
https://huagongshe.com/reaction/221425
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxide (P4O10) | HCID 14812 | — |
| Reactant | Acetamide, 2,2,2-trifluoro-N-(2-pyrazinylmethyl)- | HCID 57518396 | — |
| Solvent | Phosphorus oxychloride | HCID 24813 | — |
| Product | 3-(Trifluoromethyl)imidazo[1,5-a]pyrazine | HCID 34176321 | 65% |
Reaction Steps
2,2,2-Trifluoro-N-pyrazin-2-ylmethyl-acetamide 1i (21.0 g, 100 mmol) was added into a reaction flask at room temperature, followed by addition of 100 mL of phosphorus oxychloride. After stirring at room temperature for 30 minutes, phosphorous pentoxide (17.8 g, 125 mmol) was added to the solution. The reaction mixture was heated to reflux for 5 hours and monitored by thin layer chromatography until the disappearance of the starting materials. Phosphorus oxychloride was removed, and the reaction system was quenched with deionized water. The mixture was adjusted to pH 5-6 with 20% sodium hydroxide solution in an ice-water bath. The mixture was extracted with ethyl acetate (250 mL×4), and the combined organic phase was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography to obtain the title compound 3-trifluoromethyl-imidazo[1,5-a]pyrazine 1j (12.0 g, yield 65%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08207161B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-a0aa213f278742b9afba71d98978bd61 |
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| Source note | uspto-grants-2012_06 |
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