HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methylpiperazine → HCID 13464029, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | HCID 13464028 | HCID 13464028 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 13464029 | HCID 13464029 | — |
Reaction Steps
A mixture of 5-bromo-11-methylenebenzo[5,6]cyclohepta[1,2-c]pyridine (11.0 g.), 1-methylpiperazine (7.8 ml.), potassium tert.-butoxide (8.4 g.) and tert.-butanol (150 ml.) is heated under reflux for 4 hours. The tert.-butanol is removed in vacuo and the residue is taken up in methylene chloride (600 ml.). The resulting mixture is washed with 10% NaCl solution, saturated NaCl solution, and dried (anhydrous Na2SO4). Filtration and removal of the solvent gives 10.76 g. of dark amber oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04229455 |
| Source dataset | uspto-grants-1980_10 |
| ORD ID | ord-d81c832b41404041ab5288e266f847b3 |
| Source note | uspto-grants-1980_10 |