Hydrochloric Acid → HCID 20258991, compound
Reaction equation
[OH:1][CH:2]1[CH2:7][CH2:6][N:5]([C:8]2[C:17]([F:18])=[CH:16][C:15](N)=[C:14]3[C:9]=2[CH:10]=[CH:11][C:12]([CH3:20])=[N:13]3)[CH2:4][CH2:3]1.[ClH:21].N([O-])=O.[Na+].[OH-].[Na+]>O.C(O)CCCCCCC.[Cu]>[OH:1][CH:2]1[CH2:7][CH2:6][N:5]([C:8]2[C:17]([F:18])=[CH:16][C:15]([Cl:21])=[C:14]3[C:9]=2[CH:10]=[CH:11][C:12]([CH3:20])=[N:13]3)[CH2:4][CH2:3]1Participants
Procedure
5-(4-Hydroxy-1-piperidyl)-6-fluoro-8-aminoquinaldine (2.0 g) was dissolved in 7 ml of water and 20 ml of concentrated hydrochloric acid and 0.53 g of sodium nitrite in 3 ml of an aqueous solution was added dropwise to the solution at 0° C. After 5 minutes, one drop of n-octanol (defoaming agent) and then 0.46 g of copper powder were added to the mixture at a time. Foaming was observed immediately. After foaming stopped the reaction mixture was stirred for additional 3 minutes at 0°-5° C. The reaction mixture was diluted with water and rendered alkaline with an aqueous sodium hydroxide solution to precipitate solids which were then collected by filtration and dissolved in mixed solvent of methanol-chloroform to remove insoluble substances. After concentration, the residue was purified through silica gel column chromatography (chloroform:methanol=5:1) to give 1.62 g of 5-(4-hydroxy-1-piperidyl)-6-fluoro-8-chloroquinaldine.
Workup
- customto precipitate solids which
- filtrationwere then collected by filtration
- dissolutiondissolved in mixed solvent of methanol-chloroform
- customto remove insoluble substances
- concentrationAfter concentration
- customthe residue was purified through silica gel column chromatography (chloroform:methanol=5:1)
Sources & evidence
- ORD record
- ord-16b0ae4cdbba4fa787d5d583850da20a
- Source dataset
- uspto-grants-1983_08
- Patent number
- US04399134
Reaction notes
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