Hydrochloric Acid → HCID 13971534, compound
Reaction equation
Cl.[Cl:2][C:3]1[CH:8]=[CH:7][C:6]([C:9](=[O:24])[CH:10]([CH2:14][CH:15]2[C:20](=[O:21])[CH:19]3[CH2:22][CH2:23][N:16]2[CH2:17][CH2:18]3)C(=O)C)=[CH:5][C:4]=1[N+:25]([O-:27])=[O:26].Cl>>[ClH:2].[Cl:2][C:3]1[CH:8]=[CH:7][C:6]([C:9](=[O:24])[CH2:10][CH2:14][CH:15]2[C:20](=[O:21])[CH:19]3[CH2:22][CH2:23][N:16]2[CH2:17][CH2:18]3)=[CH:5][C:4]=1[N+:25]([O-:27])=[O:26]Participants
3
Procedure
In a manner similar to Example XXVI react 1-(4-chloro-3-nitrophenyl)-2-[(3-oxo-1-azabicyclo[2.2.2]oct-2-yl)methyl]-1,3-butanedione hydrochloride in refluxing concentrated hydrochloric acid to afford the title compound.
Sources & evidence
- ORD record
- ord-8f0c313cac4044aa8c408909f5dd95a4
- Source dataset
- uspto-grants-1986_07
- Patent number
- US04599344
Reaction notes
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