Water → HCID 19038972, compound
Reaction equation
[CH3:1][C:2]1[N:3]([CH2:27][CH2:28][C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)[C:4]2[CH:9]=[C:8]([CH3:10])[N:7]=[C:6]([N:11](CC3C=CC=CC=3)CC3C=CC=CC=3)[C:5]=2[N:26]=1.C(=O)(O)[O-].[Na+].O>C(O)=O.CO.[OH-].[OH-].[Pd+2]>[CH3:1][C:2]1[N:3]([CH2:27][CH2:28][C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)[C:4]2[CH:9]=[C:8]([CH3:10])[N:7]=[C:6]([NH2:11])[C:5]=2[N:26]=1Participants
Procedure
Palladium hydroxide on carbon (0.5 g, Pearlman's catalyst) was added to a mixture of 2,6-dimethyl-1-(2-phenylethyl)-N4,N4 -bis(phenylmethyl)-1H-imidazo[4,5-c]pyridin-4-amine (2.3 g, 5.15 mmole) in formic acid (10 mL). The reaction mixture was heated at reflux overnight. An additional 0.5 g of catalyst was added and refluxing was continued overnight. The reaction mixture was neutralized with saturated sodium bicarbonate solution, diluted with methanol then filtered through a layer of celite to remove the catalyst. The celite layer was flushed with methylene chloride and methanol. The filtrates were combined and concentrated under vacuum to provide a mixture of water and a solid. This mixture was extracted with methylene chloride. The extract was washed with water, dried over magnesium sulfate and concentrated under vacuum to provide 1.2 g of a tan solid. This solid was recrystallized from ethanol to provide 0.24 g of the desired product as a solid, m.p. 185°-187° C. Analysis: Calculated for C16H18N4 : % C, 72.15; % H, 6.81; % N, 21.04; Found: % C, 71.51; % H, 6.88; % N, 20.61.
Workup
- temperatureThe reaction mixture was heated
- temperatureat reflux overnight
- temperaturerefluxing
- filtrationthen filtered through a layer of celite
- customto remove the catalyst
- customThe celite layer was flushed with methylene chloride and methanol
- concentrationconcentrated under vacuum
- customto provide
- extractionThis mixture was extracted with methylene chloride
- washThe extract was washed with water
- dry with materialdried over magnesium sulfate
- concentrationconcentrated under vacuum
Sources & evidence
- ORD record
- ord-67d85481d57e47b38d2acf82f9588c7a
- Source dataset
- uspto-grants-1996_02
- Patent number
- US05494916
Reaction notes
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