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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

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, 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08518946B2
Source datasetuspto-grants-2013_08
ORD IDord-3c4c193d0d674e12a8f6dd64025c14d5
Source noteuspto-grants-2013_08