[3-(4-Chlorophenyl)propyl]methylamine → HCID 178483357, compound
Reaction equation
[N:1]1[C:5]2[CH2:6][CH2:7][CH:8]([C:10]([OH:12])=O)[CH2:9][C:4]=2[NH:3][CH:2]=1.[Cl:13][C:14]1[CH:19]=[CH:18][C:17]([CH2:20][CH2:21][CH2:22][NH:23][CH3:24])=[CH:16][CH:15]=1>>[ClH:13].[Cl:13][C:14]1[CH:15]=[CH:16][C:17]([CH2:20][CH2:21][CH2:22][N:23]([CH3:24])[C:10]([CH:8]2[CH2:7][CH2:6][C:5]3[NH:1][CH:2]=[N:3][C:4]=3[CH2:9]2)=[O:12])=[CH:18][CH:19]=1Participants
3
Procedure
By a similar procedure as described in Example 65, the title compound was prepared from 4,5,6,7-tetrahydrobenzimidazole-5-carboxylic acid and 3-(4-chlorophenyl)propylmethylamine.
Sources & evidence
- ORD record
- ord-e68ea76b046a41b581efd193033b17c7
- Source dataset
- uspto-grants-2002_08
- Patent number
- US06437147B1
Reaction notes
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