HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 417989Generated: October 26, 2026
1-Methylpiperazine → 1-{2,2-Dimethyl-3-[4-(4-chlorophenyl)piperazin-1-yl]-3-oxopropyl}-4-methylpiperazine
https://huagongshe.com/reaction/417989
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | 3-Bromo-1-(4-chlorophenyl)piperazine 2,2-dimethylpropan-1-one | HCID 86635776 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 1-{2,2-Dimethyl-3-[4-(4-chlorophenyl)piperazin-1-yl]-3-oxopropyl}-4-methylpiperazine | HCID 57955469 | 36.4% |
Reaction Steps
3-Bromo-1-(4-chlorophenyl)piperazine-2,2-dimethylpropan-1-one (0.87 g, 2.43 mmol) was dissolved in N-methylpyrrolidinone (3 mL). N-Methylpiperazine (0.54 mL, 4.85 mmol) was added and the reaction mixture was heated at 200° C. for 15 minutes in a Biotage Initiator microwave at normal absorption. The reaction mixture was purified by reverse phase column chromatography (gradient eluting with MeOH in water, with 1% formic acid in each solvent, 0-30%). The resulting residue was dissolved in DCM (100 mL) and stirred with solid K2CO3 for 20 minutes, filtered and concentrated ill vacuo, to give a pale brown oil which was recrystallised from heptane to give 1-{2,2-dimethyl-3-[4-(4-chlorophenyl)piperazin-1-yl]-3-oxopropyl}-4-methylpiperazine (335 mg, 36.4%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08093248B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-28e102905237482f8250978e55f8f63a |
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| Source note | uspto-grants-2012_01 |
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