Sodium Hydroxide → HCID 23696727, compound
Reaction equation
Cl.Cl.[C:3]1([CH:9]([C:38]2[CH:43]=[CH:42][CH:41]=[CH:40][CH:39]=2)[O:10][CH:11]2[CH2:16][CH2:15][N:14]([CH2:17][CH2:18][CH2:19][CH2:20][C:21]3[CH:22]=[CH:23][C:24]4[N:25]([CH:27]=[C:28]([C:30]([CH3:37])([CH3:36])[C:31]([O:33]CC)=[O:32])[N:29]=4)[N:26]=3)[CH2:13][CH2:12]2)[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[OH-].[Na+:45]>C(O)C>[C:38]1([CH:9]([C:3]2[CH:4]=[CH:5][CH:6]=[CH:7][CH:8]=2)[O:10][CH:11]2[CH2:12][CH2:13][N:14]([CH2:17][CH2:18][CH2:19][CH2:20][C:21]3[CH:22]=[CH:23][C:24]4[N:25]([CH:27]=[C:28]([C:30]([CH3:37])([CH3:36])[C:31]([O-:33])=[O:32])[N:29]=4)[N:26]=3)[CH2:15][CH2:16]2)[CH:43]=[CH:42][CH:41]=[CH:40][CH:39]=1.[Na+:45]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
631 mg of ethyl 2-[6-[4-[4-(diphenylmethoxy)piperidino]butyl]imidazo[1,2-b]pyridazin-2-yl]-2-methylpropionate dihydrochloride was dissolved in 4 ml of ethanol; 5.5 ml of a 1 N aqueous solution of sodium hydroxide was added, followed by thermal refluxing for 3 hours. After cooling, the mixture was concentrated under reduced pressure. The residue was diluted with water and adjusted to pH 5.5 by the addition of 1 N hydrochloric acid. Acetone was added to cause crystallization; the crystal precipitated was washed with water-acetone (2:1) and dried to yield 345 mg of the title compound.
Workup
- customrefluxing for 3 hours
- temperatureAfter cooling
- concentrationthe mixture was concentrated under reduced pressure
- additionThe residue was diluted with water
- additionadjusted to pH 5.5 by the addition of 1 N hydrochloric acid
- additionAcetone was added
- customcrystallization
- customthe crystal precipitated
- washwas washed with water-acetone (2:1)
- customdried
Sources & evidence
- ORD record
- ord-a98cbd9e703449d0a2027a5f09b9bfcc
- Source dataset
- uspto-grants-2003_09
- Patent number
- US06627630B1
Reaction notes
Loading…