Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 14726462 | HCID 14726462 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 14726463 | HCID 14726463 | 99.7% |
Reaction Steps
4.00 g (0.00985 mol) of 6-chloro-3-methoxy-4-((4-(4-(2-methoxyphenyl)-1-piperazinyl)butyl)amino)-pyridazine are dissolved in 40 ml of glacial acetic acid, and 40 ml of 63% strength HBr are added. The mixture is refluxed for 2 hours, 200 ml of water are added, 30% strength KOH is added to pH 6, and the precipitated substance is filtered off with suction and thoroughly washed with water. 3.85 g (99.7% of theory) of 6-chloro-4-((4-(4-(2-methoxyphenyl)-1-piperazinyl)butyl)amino)-3(2H)-pyridazinone are obtained, purified by recrystallization from ethanol with addition of charcoal, and immediately added to a solution of ethanolic hydrochloric acid, resulting in 3.26 g (68.7% of theory) of pure dihydrochloride, m.p. 247°-252° C.; C 47.2%, H 6.0%, Cl(tot) 21.9%, Cl- 14.6%, N 14.4%, O 10.0%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05034391 |
|---|
| Source dataset | uspto-grants-1991_07 |
|---|
| ORD ID | ord-4d33a44c5e7448c58334105eb232e976 |
|---|
| Source note | uspto-grants-1991_07 |
|---|