Water → HCID 11516277, compound
Reaction equation
[H-].[Al+3].[Li+].[H-].[H-].[H-].[CH2:7]([N:14]1[CH2:19][CH2:18][CH:17]([N:20]=[C:21]([C:28]2[CH:29]=[N:30][CH:31]=[CH:32][C:33]=2[NH2:34])[C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[CH2:16][CH2:15]1)[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.O.[OH-].[Na+]>O1CCCC1>[CH2:7]([N:14]1[CH2:19][CH2:18][CH:17]([NH:20][CH:21]([C:28]2[CH:29]=[N:30][CH:31]=[CH:32][C:33]=2[NH2:34])[C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[CH2:16][CH2:15]1)[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
To a suspension of 0.68 g (17.9 mmol) of lithium aluminum hydride in 100 mL of tetrahydrofuran was added dropwise a solution of 6.65 g (17.9 mmol) of 3-[α-{(1-benzylpiperidin-4-yl)imino}benzyl]-4-aminopyridine in tetrahydrofuran 30 ml under reflux, and the mixture was heated under reflux for 1 hour. After being cooled, the mixture was added sequentially with 0.7 mL of water, 0.7 mL of an aqueous 15% sodium hydroxide solution and 2 mL of water, under ice-cooling. After being stirred for 1 hour at ambient temperature, the reaction mixture was filtered through cerite. The filtrate was concentrated and the residue was purified by means of column chromatography (silica gel, 1:9 methanol:chloroform) to give 4.2 g (11.3 mmol) of the title compound.
Workup
- temperatureunder reflux
- temperaturethe mixture was heated
- temperatureunder reflux for 1 hour
- temperatureAfter being cooled
- temperaturecooling
- filtrationthe reaction mixture was filtered through cerite
- concentrationThe filtrate was concentrated
- customthe residue was purified by means of column chromatography (silica gel, 1:9 methanol:chloroform)
Sources & evidence
- ORD record
- ord-063b756c294848609f74b86144edd1a4
- Source dataset
- uspto-grants-1996_09
- Patent number
- US05556860
Reaction notes
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