HCID 178509760, compound → Benzonitrile, 4-(5,6,7,8-tetrahydroimidazo(1,5-a)pyridin-5-yl)-, hydrochloride (1:1)
Reaction equation
[Cl:1][CH:2]([C:11]1[CH:16]=[CH:15][C:14]([C:17]#[N:18])=[CH:13][CH:12]=1)[CH2:3][CH2:4][CH2:5][C:6]1[N:7]=[CH:8][NH:9][CH:10]=1>C(Cl)(Cl)Cl>[ClH:1].[C:17]([C:14]1[CH:15]=[CH:16][C:11]([CH:2]2[N:7]3[CH:8]=[N:9][CH:10]=[C:6]3[CH2:5][CH2:4][CH2:3]2)=[CH:12][CH:13]=1)#[N:18]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 2.0 g of 4-(4-chloro-4-p-cyanophenyl-n-butyl)-1H-imidazole in 50 ml of chloroform is refluxed for 4 hours under nitrogen, cooled and evaporated to yield the title compound.
Workup
- temperaturecooled
- customevaporated
Sources & evidence
- ORD record
- ord-a13d2fc26be4468ba5b635a2fcb23441
- Source dataset
- uspto-grants-1986_10
- Patent number
- US04617307
Reaction notes
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