Hydrochloric Acid → HCID 19823303, compound
Reaction equation
[ClH:1].[CH3:2][C:3]1[N:7]2[CH:8]=[CH:9][C:10]([CH3:12])=[CH:11][C:6]2=[N:5][C:4]=1[CH2:13][CH2:14][C:15]1[CH:24]=[CH:23][C:18]2[N:19]=[C:20]([NH2:22])[O:21][C:17]=2[CH:16]=1>C(O)C>[ClH:1].[ClH:1].[CH3:2][C:3]1[N:7]2[CH:8]=[CH:9][C:10]([CH3:12])=[CH:11][C:6]2=[N:5][C:4]=1[CH2:13][CH2:14][C:15]1[CH:24]=[CH:23][C:18]2[N:19]=[C:20]([NH2:22])[O:21][C:17]=2[CH:16]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Conc. hydrochloric acid (1.1 ml) was added to a mixture of 6-[2-(3,7-dimethylimidazo[1,2-a]pyridin-2-yl)ethyl]-2-aminobenzoxazole (1.5 g) in ethanol (9 ml) and the mixture was stirred for 5 minutes at ambient temperature. The isolated crystal was collected by filtration and the resulting crystal was recrystallized from a mixture of ethanol and ethyl acetate to give 6-[2-(3,7-dimethylimidazo[1,2-a]pyridin-2-yl)ethyl]-2-aminobenzoxazole dihydrochloride (0.91 g).
Workup
- filtrationThe isolated crystal was collected by filtration
- customthe resulting crystal was recrystallized from a mixture of ethanol and ethyl acetate
Sources & evidence
- ORD record
- ord-f45f405398684f4f973d88b4ea97eaff
- Source dataset
- uspto-grants-1991_09
- Patent number
- US05047411
Reaction notes
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