HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methylpiperazine → HCID 12781932, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | HCID 12781927 | HCID 12781927 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 12781932 | HCID 12781932 | 73.9% |
Reaction Steps
2-[5-(Bromomethyl)-2-thienyl]-5-nitrobenzoxazole (1.16 g, 0.0034 mole, prepared as described in Example 1) and N-methylpiperazine (1.4 g, 0.014 mole) are dissolved in 50 ml of benzene and heated at reflux for 24 hours. The precipitated N-methylpiperazine hydrobromide is removed by filtration and the benzene removed under vacuum yielding a solid. Crystallization from ethanol yields 0.9 g of the title compound, melting point 135°-137°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03969351 |
| Source dataset | uspto-grants-1976_07 |
| ORD ID | ord-0171cdeb080348eea407adcce92dae27 |
| Source note | uspto-grants-1976_07 |