HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493330Generated: October 30, 2026
Diphenyl Ether → 4-Benzyl-1-(3-chloro-2-pyrazinyl)-cis-2,6-dimethylpiperazine
https://huagongshe.com/reaction/493330
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diphenyl Ether | HCID 7583 | — |
| Reactant | Tributylamine | HCID 7622 | — |
| Reactant | 2,3-Dichloropyrazine | HCID 78575 | — |
| Reactant | (3r,5s)-1-Benzyl-3,5-dimethylpiperazine | HCID 12197174 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Benzyl-1-(3-chloro-2-pyrazinyl)-cis-2,6-dimethylpiperazine | HCID 53660138 | — |
Reaction Steps
A mixture of 2,3-dichloropyrazine (4.9 g, 32.9 mmol), 1-benzyl-cis-3,5-dimethylpiperazine (5.9 g, 29.0 mmol), tributylamine (5.9 g, 32 mmol) and diphenyl ether (70 mL) was heated in a sealed tube at 220° C. for 3 days. The reaction mixture was cooled to ambient temperature and EtOAc (200 mL) and toluene (100 mL) were added. The organic phase was extracted with 5 M aqueous HCl (×3) and the combined aqueous phases were extracted with CHCl3 (×3). The combined organic layers, which contained the product, were washed with aqueous NaOH (5 M), dried (MgSO4), and the solvent was evaporated. The crude product (0.96 g), about 80% pure based on GC, was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07534794B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-70452dfa31b140209022565b4cb90eb8 |
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| Source note | uspto-grants-2009_05 |
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