Hydrochloric Acid → HCID 21284872, compound
Reaction equation
[C:1]1(=[O:19])[N:5]([CH2:6][C:7](=O)[CH2:8][CH2:9][C:10](=O)[CH3:11])[C:4](=[O:14])[C:3]2=[CH:15][CH:16]=[CH:17][CH:18]=[C:2]12.[N:20]1([CH2:25][CH2:26][CH2:27][NH2:28])[CH:24]=[CH:23][N:22]=[CH:21]1.[ClH:29]>C(O)(=O)C>[ClH:29].[N:20]1([CH2:25][CH2:26][CH2:27][N:28]2[C:10]([CH3:11])=[CH:9][CH:8]=[C:7]2[CH2:6][N:5]2[C:4](=[O:14])[C:3]3=[CH:15][CH:16]=[CH:17][CH:18]=[C:2]3[C:1]2=[O:19])[CH:24]=[CH:23][N:22]=[CH:21]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
5.2 g (0.02 mol) of 6-phthalimido-2,5-hexanedione and 2.5 g (0.02 mol) of 3-(1-imidazolyl)-propylamine are stirred in 70 ml of acetic acid at 80° C. for 2 hours and the mixture is worked up as in Example 1. After ethanolic hydrochloric acid has been added, the product is filtered off and recrystallised from ethanol.
Workup
- filtrationthe product is filtered off
- customrecrystallised from ethanol
Sources & evidence
- ORD record
- ord-efdaa5cb6e5b4c979265bfeeb3b3bbaf
- Source dataset
- uspto-grants-1988_11
- Patent number
- US04785010
Reaction notes
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