HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 737127Generated: October 31, 2026
Methyl iodide → (4-Methyl-3-phenyl-piperazin-1-yl)-(2'-trifluoromethyl-biphenyl-4-yl)-methanone
https://huagongshe.com/reaction/737127
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 57849547 | HCID 57849547 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (4-Methyl-3-phenyl-piperazin-1-yl)-(2'-trifluoromethyl-biphenyl-4-yl)-methanone | HCID 57849491 | — |
Reaction Steps
This compound could be made in the following manner: 100 mg of (3-phenyl-piperazin-1-yl)-(2′-trifluoromethyl-biphenyl-4-yl)-methanone would be dissolved in 3 mL of acetonitrile, 2 equiv. of N,N-diisopropylethylamine would be added followed by 1.1 equiv. of iodomethane. The reaction would be heated to 80° C. overnight. After cooling to room temperature, the reaction would be diluted with dichloromethane and washed with 1M aqueous sodium hydroxide solution, dried over sodium sulfate and concentrated in vacuo. The crude residue would be purified by column chromatography to afford the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07595397B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-2e91792237974161a3b22a1bb6a892a9 |
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| Source note | uspto-grants-2009_09 |
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