HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1896092Generated: November 1, 2026
Phosphorus oxide (P4O10) → 3-(Trifluoromethyl)imidazo[1,5-a]pyrazine
https://huagongshe.com/reaction/1896092
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, followed by addition of 100 mL of phosphorus oxychloride. After stirring 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. The mixture was concentrated under reduced pressure, 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 and then extracted with ethyl acetate (250 mL×4). The combined organic phase was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The resulting residues were purified by silica gel column chromatography with system A as eluant to obtain the title compound 3-trifluoromethyl-imidazo[1,5-a]pyrazine 1j (12.0 g, yield 65%) as a yellow solid. MS m/z (ESI): 188.0 [M+1]. 1H NMR (400 MHz, CDCl3, ppm): δ 9.15 (s, 1H), 8.06 (d, 1H), 7.92 (s, 1H), 7.81 (d, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08518946B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-3c4c193d0d674e12a8f6dd64025c14d5 |
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| Source note | uspto-grants-2013_08 |
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