Sodium Acetate → 4-(Piperazin-1-yl)pyridazine
Reaction equation
Cl[C:2]1[N:3]=[N:4][C:5](Cl)=[CH:6][C:7]=1[N:8]1[CH2:13][CH2:12][NH:11][CH2:10][CH2:9]1.C([O-])(=O)C.[Na+]>CO.[Pd]>[N:8]1([C:7]2[CH:6]=[CH:5][N:4]=[N:3][CH:2]=2)[CH2:9][CH2:10][NH:11][CH2:12][CH2:13]1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
9.3 g 3,6-dichloro-4-piperazin-1-yl-pyridazine (cf. 10.2) and 6.5 g sodium acetate are suspended in 100 ml of methanol and hydrogenated with 1 g Pd/C 10% at ambient temperature. The catalyst is suction filtered and the filtrate is evaporated to dryness. The product is extracted with chloroform, washed with sodium hydroxide solution and precipitated as the hydrochloride with an ethereal HCl solution. 8.6 g (V-4) are obtained. M.p.>300° C.
Workup
- filtrationfiltered
- customthe filtrate is evaporated to dryness
- extractionThe product is extracted with chloroform
- washwashed with sodium hydroxide solution
- customprecipitated as the hydrochloride with an ethereal HCl solution
- custom8.6 g (V-4) are obtained
Sources & evidence
- ORD record
- ord-6092abd564e44c578aaa1d89b47fa14a
- Source dataset
- uspto-grants-2014_06
- Patent number
- US08759326B2
Reaction notes
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