HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methylpiperazine → HCID 57066993, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | HCID 57037835 | HCID 57037835 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 57066993 | HCID 57066993 | 86.6% |
Reaction Steps
A stirred solution of 1-phenylmethyleneamino-3-(4-iodobutyl)-2-imidazolidinone (10.0 g, 0.0269 mole), dimethylformamide (150 ml) and 1-methylpiperazine (6.0 ml, 3.4 g, 0.0539 mole) is heated to reflux. Reflux is maintained for 2.5 hours. The solution is concentrated under reduced pressure to a semi-solid residue. This residue is dissolved in CHCl3 (300 ml), then washed with saturated NaHCO3 solution. (3×400 ml), H2O (2×100 ml) and dried over MgSO4. The filtered solution is concentrated under reduced pressure to an oily residue. This residue is triturated in hexane (300 ml) by stirring. The solid is collected and air-dried to give 8.0 g (0.0233 mole) of 1-phenylmethyleneamino-3-[4-(4-methyl-1-piperazinyl)butyl]-2-imidazolidinone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06083945 |
| Source dataset | uspto-grants-2000_07 |
| ORD ID | ord-aaee0fb608b041ecb1f6d4b2762e38b8 |
| Source note | uspto-grants-2000_07 |