Ethanol → HCID 9828495, compound
Reaction equation
[ClH:1].C(OCC)(=O)C.[CH3:8][N:9]1[CH2:14][CH2:13][N:12]([C:15]([C:17]2[N:21]([CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH3:39])[C:20]3[CH:40]=[CH:41][CH:42]=[CH:43][C:19]=3[N:18]=2)=[O:16])[CH2:11][CH2:10]1.C(O)C>C(OCC)(=O)C>[ClH:1].[CH3:8][N:9]1[CH2:10][CH2:11][N:12]([C:15]([C:17]2[N:21]([CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH3:39])[C:20]3[CH:40]=[CH:41][CH:42]=[CH:43][C:19]=3[N:18]=2)=[O:16])[CH2:13][CH2:14]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
4N Hydrochloric acid/ethyl acetate solution (0.18 ml) was added to a solution containing 2-[(4-methylpiperazinyl)carbonyl]-1-octadecyl-1H-benzimidazole (0.348 g) in ethyl acetate (4 ml) and the mixture was stirred for 15 minutes at room temperature. The reaction mixture, with ethanol (1 ml) and ethyl acetate (4 ml) added thereto, was dissolved by heating, and then cooled with ice. The depositing crystals were collected by filtration, thereby yielding the entitled compound (0.318 g) as white solid.
Workup
- dissolutionwas dissolved
- temperatureby heating
- temperaturecooled with ice
- filtrationThe depositing crystals were collected by filtration
Sources & evidence
- ORD record
- ord-e6cf557529fc4dc0adbbd1322c27ed51
- Source dataset
- uspto-grants-2001_03
- Patent number
- US06204264B1
Reaction notes
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