HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1784708Generated: October 28, 2026
1-Methylpiperazine → 1,1-Dimethylethyl 3-[4-(4-methyl-1-piperazinyl)phenyl]-1-piperidinecarboxylate
https://huagongshe.com/reaction/1784708
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | 2-(Di-tert-butylphosphino)biphenyl | HCID 2734215 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | tert-Butyl 3-(4-bromophenyl)piperidine-1-carboxylate | HCID 46840041 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1,1-Dimethylethyl 3-[4-(4-methyl-1-piperazinyl)phenyl]-1-piperidinecarboxylate | HCID 53628953 | 63.2% |
Reaction Steps
To a suspension of 3-(4-bromophenyl)-piperidine-1-carboxylic acid tert-butyl ester (3.0 g, 8.8 mmol), palladium acetate (80 mg, 0.36 mmol), 2-(di-t-butyl phosphino)biphenyl (210 mg, 0.70 mmol), and sodium t-butoxide (1.2 g, 125 mmol) in toluene (30 mL) was added N-methylpiperazine (1.3 g, 13.0 mmol) at room temperature. After heating at 90° C. for 5 h, the resulting suspension was passed through a Celite column. The filtrate was concentrated under reduced pressure, and the residue was purified by silica gel chromatography eluting 5-25% of ethyl acetate in hexane to afford 3-(4-(4-methylpiperazin-1-yl)-phenyl)-piperidine-1-carboxylic acid tert-butyl ester (2.0 g, 5.56 mmol, 63%) as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07504411B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-63f98dd0911049c8ac37e68b334e3a3e |
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| Source note | uspto-grants-2009_03 |
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