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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1896093Generated: November 1, 2026

3-(Trifluoromethyl)imidazo[1,5-a]pyrazine → 5,6,7,8-Tetrahydro-3-(trifluoromethyl)imidazo[1,5-a]pyrazine

https://huagongshe.com/reaction/1896093

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)imidazo[1,5-a]pyrazineHCID 34176321—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product5,6,7,8-Tetrahydro-3-(trifluoromethyl)imidazo[1,5-a]pyrazineHCID 3417631499.4%

Reaction Steps

3-Trifluoromethyl-imidazo[1,5-a]pyrazine 1j (12.0 g, 64.2 mmol) was dissolved in 150 mL of anhydrous ethanol, then 10% Pd/C (500 mg) was added to the solution. The reaction mixture was stirred at room temperature under a hydrogen atmosphere for 12 hours. The reaction solution was filtered through a pad of coarse silica gel and the filtrate was concentrated under reduced pressure to obtain the title compound 3-trifluoromethyl-5,6,7,8-tetrahydro-imidazo[1,5-a]pyrazine 1k (12.2 g, yield 99%) as a brown solid. 1H NMR (400 MHz, CDCl3, ppm): δ 6.84 (s, 1H), 4.10 (m, 4H), 3.26 (m, 2H), 1.81 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08518946B2
Source datasetuspto-grants-2013_08
ORD IDord-e3de90ed91054799bd3515efc3c866ef
Source noteuspto-grants-2013_08