HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 737137Generated: October 30, 2026
Methyl iodide → 1-Methyl-2-phenyl-4-(2'-chloro-5'-methyl-biphenyl-4-ylmethyl)-piperazine
https://huagongshe.com/reaction/737137
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 57849521 | HCID 57849521 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Methyl-2-phenyl-4-(2'-chloro-5'-methyl-biphenyl-4-ylmethyl)-piperazine | HCID 57849650 | — |
Reaction Steps
This compound could be made the following manner: 100 mg of 3-benzyl-1-(2′-chloro-5′-methyl-biphenyl-4-ylmethyl)-piperazine would be dissolved in acetonitrile, 3 equiv. of N,N-diisopropylethylamine would be added followed by 1.1 equiv. of iodomethane. The reaction would be stirred at 80° C. overnight. The reaction would be diluted with dichloromethane and washed with 1N aqueous NaOH solution. The organic layer would be dried over Na2SO4, filtered and concentrated in vacuo. The crude residue would be purified by column chromatography to afford 1-methyl-2-phenyl-4-(2′-chloro-5′-methyl-biphenyl-4-ylmethyl)-piperazine.
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-c0c205d68ac345f886eea1d2f4e8253d |
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| Source note | uspto-grants-2009_09 |
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