HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3'-(4-Trifluoromethyl-phenyl)-3,4,5,6-tetrahydro-2H-[1,2']bipyrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 2-Chloro-3-(4-chlorophenyl)pyrazine | HCID 13199889 | — |
| Reactant | 2-Chloro-3-(4-trifluoromethylphenyl)-pyrazine | HCID 65645518 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3'-(4-Trifluoromethyl-phenyl)-3,4,5,6-tetrahydro-2H-[1,2']bipyrazine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08202873B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-29880e8cc25447a285e1bf5147b5b193 |
| Source note | uspto-grants-2012_06 |