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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220425Generated: October 30, 2026

Water → 3'-(4-Trifluoromethyl-phenyl)-3,4,5,6-tetrahydro-2H-[1,2']bipyrazine

https://huagongshe.com/reaction/220425

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPiperazineHCID 4837—
Reactant2-Chloro-3-(4-chlorophenyl)pyrazineHCID 13199889—
Reactant2-Chloro-3-(4-trifluoromethylphenyl)-pyrazineHCID 65645518—
SolventDichloromethaneHCID 6344—
Product3'-(4-Trifluoromethyl-phenyl)-3,4,5,6-tetrahydro-2H-[1,2']bipyrazineHCID 68594838—

Reaction Steps

Prepare 2-chloro-3-(4-trifluoromethylphenyl)-pyrazine in 30% according to the procedure used to make 2-chloro-3-(4-chlorophenyl)-pyrazine. Couple 2-chloro-3-(4-trifluoromethylphenyl)-pyrazine (0.570 g, 2.20 mmol) and piperazine (4.31 g, 50.0 mmol), at 125° C. for 111 min. Cool the reaction to about 70° C., add water (50 mL), stir until the reaction temperature is below 35° C. and dilute with DCM (70 mL). Separate the layers, extract the aqueous layer with DCM (2×70 mL), wash the combined organic layers with saturated aqueous sodium chloride, dry (magnesium sulfate), concentrate and purify (silica gel chromatography, eluting with 0:100 to 1:1 ethyl acetate:hexanes), to give the title preparation (0.384 g, 57%). MS (ES): m/z=309 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202873B2
Source datasetuspto-grants-2012_06
ORD IDord-29880e8cc25447a285e1bf5147b5b193
Source noteuspto-grants-2012_06