HCID 9845444, compound → HCID 9912263, compound
Reaction equation
[ClH:1].C(OCC)(=O)C.[CH2:8]([C:25]1[N:29]([CH2:30][CH2:31][N:32]([CH3:34])[CH3:33])[C:28]2[CH:35]=[CH:36][CH:37]=[CH:38][C:27]=2[N:26]=1)[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24]>C(OCC)(=O)C>[ClH:1].[CH2:8]([C:25]1[N:29]([CH2:30][CH2:31][N:32]([CH3:33])[CH3:34])[C:28]2[CH:35]=[CH:36][CH:37]=[CH:38][C:27]=2[N:26]=1)[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
4N Hydrochloric acid/ethyl acetate solution (0.12 ml) was added to a solution containing 2-(2-heptadecyl-1H-benzimidazol-1-yl)-N,N-dimethyl-1-ethanamine (0.200 g) in ethyl acetate (2 ml). After being stirred for 15 minutes at room temperature, the reaction mixture was concentrated. The residue was recrystallized with the mixed solution of ethanol-ethyl acetate, thereby yielding the entitled compound (0.182 g) as white solid.
Workup
- concentrationthe reaction mixture was concentrated
- customThe residue was recrystallized with the mixed solution of ethanol-ethyl acetate
Sources & evidence
- ORD record
- ord-b1d48c1005e14ca6becc5857f3731768
- Source dataset
- uspto-grants-2001_03
- Patent number
- US06204264B1
Reaction notes
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