HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762162Generated: November 1, 2026
1-Methylpiperazine → HCID 10091734, compound
https://huagongshe.com/reaction/1762162
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | HCID 11726606 | HCID 11726606 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 10091734 | HCID 10091734 | 50.7% |
Reaction Steps
A mixture of 3-bromomethyl-4-(3-nitrophenyl)-6-phenylpyridazine (0.6 g), 1-methylpiperazine (0.36 g) in isopropyl alcohol (6 ml) was refluxed for 30 minutes. After evaporating the solvent, the residue was dissolved in methylene chloride (50 ml), washed with saturated aqueous sodium chloride and dried over magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was subjected to a column chromatography on silica gel (50 g) and eluted with a mixture of chloroform and methanol (20:1 V/V). The fractions containing the desired compound were combined and concentrated under reduced pressure. The residue was recrystallized from ethanol to give 3-(4-methylpiperazin-1-ylmethyl)-4-(3-nitrophenyl)-6-phenylpyridazine (0.32 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04831030 |
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| Source dataset | uspto-grants-1989_05 |
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| ORD ID | ord-29e08859f32e4c86828c441508df79f5 |
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| Source note | uspto-grants-1989_05 |
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