HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methylpiperazine → 5-((4-Methylpiperazine-1-yl)methyl)furan-2-carboxaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | 5-(Bromomethyl)-2-furaldehyde | HCID 11970491 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5-((4-Methylpiperazine-1-yl)methyl)furan-2-carboxaldehyde | HCID 86671381 | 55% |
Reaction Steps
To a solution of 0.20 g (1.1 mmol) of 5-(bromomethyl)furan-2-carboxaldehyde in anhydrous dioxane (10 ml) are added 261 μL (0.24 g, 2.3 mmol) of 1-methylpiperazine. The mixture is stirred at room temperature for 30 min. The precipitate formed is filtered and rinsed with dioxane. The filtrate is concentrated, dissolved in dichloromethane, and washed in water. The organic phase is dried over magnesium sulfate, filtered, and concentrated. The residue obtained is purified by chromatography on silica (eluent: 7N NH4OH in MeOH/CH2Cl2, 5:95) to yield 0.12 g (55%) of 5-((4-methylpiperazine-1-yl)methyl)furan-2-carboxaldehyde in the form of an orange solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08889711B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-c4556eb69876429c80231218238a6038 |
| Source note | uspto-grants-2014_11 |