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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxide (P4O10)HCID 14812—
ReactantAcetamide, 2,2,2-trifluoro-N-(2-pyrazinylmethyl)-HCID 57518396—
SolventPhosphorus oxychlorideHCID 24813—
Product3-(Trifluoromethyl)imidazo[1,5-a]pyrazineHCID 3417632165%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207161B2
Source datasetuspto-grants-2012_06
ORD IDord-a0aa213f278742b9afba71d98978bd61
Source noteuspto-grants-2012_06