HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Amino-4-methylpiperazine → HCID 136332143, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Amino-4-methylpiperazine | HCID 81349 | — |
| Reactant | HCID 10340441 | HCID 10340441 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 136332143 | HCID 136332143 | — |
Reaction Steps
39.15 g (0.1 mole) of 3-(4-trifluoromethylphenyl)-7-chloro-3,4-dihydroacridine-1,9(2H,10H)-dione are suspended in 500 ml of ethanol, 11.5 g (0.1 mole) of N-methyl-N'-aminopiperazine are added and the reaction mixture is heated to reflux for 90 minutes. A clear solution is formed during this. After cooling down, the ethanol is distilled out in a rotary evaporator and the solid residue is recrystallized from toluene/cyclohexane (1:1). 44 g (=90% of theory) of the title compound are thus obtained in the form of pale yellow crystals of melting point 246° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04593027 |
| Source dataset | uspto-grants-1986_06 |
| ORD ID | ord-afed0fcd249d47259e9644294d4c919b |
| Source note | uspto-grants-1986_06 |