2,3-Dichloronitrobenzene → (7-Chloro-1H-benzimidazol-1-yl)acetic acid
Reaction equation
Br[C:2]1[C:7]2[N:8]([CH2:11][C:12]([OH:14])=[O:13])[CH:9]=[N:10][C:6]=2[CH:5]=[CH:4][CH:3]=1.[Cl:15]C1C=CC=C([N+]([O-])=O)C=1Cl>>[Cl:15][C:2]1[C:7]2[N:8]([CH2:11][C:12]([OH:14])=[O:13])[CH:9]=[N:10][C:6]=2[CH:5]=[CH:4][CH:3]=1Participants
3
Procedure
Alternatively, the title compound was synthesised according to the procedure described for the synthesis of (7-bromo-1H-benzimidazol-1-yl)acetic acid (parts A-D) starting from 1,2-dichloro-3-nitrobenzene. The new intermediates isolated were:
Workup
- customThe new intermediates isolated
Sources & evidence
- ORD record
- ord-432688e682954a388ee3920837737f30
- Source dataset
- uspto-grants-2010_01
- Patent number
- US07645784B2
Reaction notes
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