HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912251Generated: November 1, 2026
Potassium Phosphate, Tribasic → N-[3-(4-Ethyl-piperazin-1-yl)-phenyl]-N-methyl-acetamide
https://huagongshe.com/reaction/912251
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 1-Ethylpiperazine | HCID 79196 | — |
| Reactant | HCID 59244769 | HCID 59244769 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | 2-Dicyclohexylphosphino-2',6'-dimethoxybiphenyl | HCID 11269872 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-[3-(4-Ethyl-piperazin-1-yl)-phenyl]-N-methyl-acetamide | HCID 59245018 | 80% |
Reaction Steps
To a DMF solution (2.5 ml) of N-(3-bromo-phenyl)-N-methyl-acetamide (114 mg) obtained in Step B, palladium acetate (1.1 mg), S-Phos (4.1 mg) and potassium phosphate (212.3 mg), 1-ethylpiperazine (76.2 μl) was added, and then the mixture was degassed under ultrasonic irradiation. This was stirred at 100° C. for 5 hours, followed by addition of water (10 ml), which was extracted with ethyl acetate (10 ml×2), and the organic layer was dried over sodium sulfate. After the sodium sulfate was filtered off, the solvent was distilled off under reduced pressure, followed by purification by silica gel column chromatography (dichloromethane/methanol=20/1 to 10/1), to obtain the desired compound (104.9 mg, 80%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08022205B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-3329d1e0981640b48e87997bce9bcb6e |
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| Source note | uspto-grants-2011_09 |
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