Water → HCID 12112231, compound
Reaction equation
[NH2:1][C:2]1[CH:3]=[C:4]([CH:11]=[CH:12][CH:13]=1)[O:5][CH2:6][CH2:7][CH2:8][NH:9][CH3:10].[O:14]=[C:15]([OH:27])[C@@H:16]([C@H:18]([C@H:20]([C@@H:22]([C:24]([OH:26])=[O:25])[OH:23])[OH:21])[OH:19])[OH:17].O>C(O)C>[O:14]=[C:15]([OH:27])[C@@H:16]([C@H:18]([C@H:20]([C@@H:22]([C:24]([OH:26])=[O:25])[OH:23])[OH:21])[OH:19])[OH:17].[NH2:1][C:2]1[CH:3]=[C:4]([CH:11]=[CH:12][CH:13]=1)[O:5][CH2:6][CH2:7][CH2:8][NH:9][CH3:10].[NH2:1][C:2]1[CH:3]=[C:4]([CH:11]=[CH:12][CH:13]=1)[O:5][CH2:6][CH2:7][CH2:8][NH:9][CH3:10]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of (3-(3-aminophenoxy)propyl)methylamine (2.77 g, 15.30 mmol) in ethanol was added galactaric acid (1.61 g, 7.65 mmol). Water was added drop-wise, while warming the solution to reflux. To remove some white, insoluble solids, the warm solution was filtered through a glass wool plug, washing the filter plug with a warm solution of ethanol-water (4:1, v/v). The filtrate was diluted with ethanol. The mixture was allowed to cool to ambient temperature and was further cooled at 5° C. No solids had formed. Consequently, the solution was concentrated to a residue that was vacuum dried. The solids were slurried in 2-propanol, and the 2-propanol was evaporated. The resulting solids were slurried in anhydrous ether. The product was filtered, washed with ether and vacuum dried at 40° C. to give 3.928 g (89.6%) of brown, powdery crystals, mp 160-1 70° C. The compound exhibits a Ki of 64 nM; the effect at muscle sites is 11 percent; and the effect at ganglia sites is 5 percent. The compound exhibits neurotransmitter release of 30 percent. The compound exhibits neurotransmitter release of 60 percent.
Workup
- temperaturewhile warming the solution
- temperatureto reflux
- customTo remove some white, insoluble solids
- filtrationthe warm solution was filtered through a glass wool plug
- washwashing the filter plug with a warm solution of ethanol-water (4:1
- additionThe filtrate was diluted with ethanol
- temperaturewas further cooled at 5° C
- customNo solids had formed
- concentrationConsequently, the solution was concentrated to a residue that
- customdried
- customthe 2-propanol was evaporated
- filtrationThe product was filtered
- washwashed with ether and vacuum
- customdried at 40° C.
- customto give 3.928 g (89.6%) of brown, powdery crystals, mp 160-1 70° C
Sources & evidence
- ORD record
- ord-2cfe465e614b47e381d37a74bce87f68
- Source dataset
- uspto-grants-2002_08
- Patent number
- US06441006B2
Reaction notes
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