HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 3,6-Dichloro-4-((4-(4-(2-methoxyphenyl)-1-piperazinyl)butyl)amino)pyridazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3,4,6-Trichloropyridazine | HCID 95123 | — |
| Reactant | 1-(4-Aminobutyl)-4-(2-methoxyphenyl)piperazine | HCID 10999903 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3,6-Dichloro-4-((4-(4-(2-methoxyphenyl)-1-piperazinyl)butyl)amino)pyridazine | HCID 14726460 | 54.2% |
Reaction Steps
9.25 g (0.050 mol) of 3,4,6-trichloropyridazine are stirred with 6.90 g (0.050 mol) of powdered anhydrous potassium carbonate and 13.15 g (0.050 mol) of 1-(4-aminobutyl)-4-(2-methoxyphenyl)piperazine in 1350 ml of dry acetonitrile at room temperature for 96 hours. The mixture is subsequently filtered with suction, and the filtrate is concentrated in vacuo. The residue is taken up in ethanol, and the trihydrochloride of 3,6-dichloro-4-((4-(4-(2-methoxyphenyl)-1-piperazinyl)butyl)amino)pyridazine of m.p.: 155°-170° C. is precipitated with ethereal HCl; yield: 54.2% of theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05034391 |
| Source dataset | uspto-grants-1991_07 |
| ORD ID | ord-e2ecf7f680624a02b4740b552ea00331 |
| Source note | uspto-grants-1991_07 |