2-Chloro-5,6-dihydro-4H-imidazo[4,5,1-ij]quinoline → HCID 19419852, compound
Reaction equation
[Cl:1][C:2]1[N:12]2[C:13]3[C:8]([CH2:9][CH2:10][CH2:11]2)=[CH:7][CH:6]=[CH:5][C:4]=3[N:3]=1>N1CCCCC1>[ClH:1].[N:12]1([C:2]2[N:12]3[C:13]4[C:8]([CH2:9][CH2:10][CH2:11]3)=[CH:7][CH:6]=[CH:5][C:4]=4[N:3]=2)[CH2:13][CH2:8][CH2:9][CH2:10][CH2:11]1Participants
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 2-chloro-5,6-dihydro-4H-imidazo[4,5,1-ij]quinoline (3.5 g) in piperidine (20 ml) was stirred under reflux, under nitrogen, for four hrs. The reaction mixture was quenched with dilute sodium bicarbonate solution (200 ml) and the aqueous suspension was extracted with chloroform. The combined organic extracts were dried over anhydrous magnesium sulfate and concentrated. The residue was purified by high performance liquid chromatography (silica gel; 3:1 dichloromethane-ethyl acetate). The appropriate fractions were collected and concentrated. This residue was dissolved in ether and treated dropwise with a solution of hydrogen chloride/ether. The precipitate was collected and washed with ether to give 4.3 g (85%) of product, mp 260° C.
Workup
- temperatureunder reflux, under nitrogen, for four hrs
- customThe reaction mixture was quenched with dilute sodium bicarbonate solution (200 ml)
- extractionthe aqueous suspension was extracted with chloroform
- dry with materialThe combined organic extracts were dried over anhydrous magnesium sulfate
- concentrationconcentrated
- customThe residue was purified by high performance liquid chromatography (silica gel; 3:1 dichloromethane-ethyl acetate)
- customThe appropriate fractions were collected
- concentrationconcentrated
- dissolutionThis residue was dissolved in ether
- additiontreated dropwise with a solution of hydrogen chloride/ether
- customThe precipitate was collected
- washwashed with ether
Sources & evidence
- ORD record
- ord-98e9f368bc87492396a943bf3dc26a59
- Source dataset
- uspto-grants-1996_10
- Patent number
- US05563272
Reaction notes
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