trans-2-Phenyl-1-cyclopropanecarbonyl chloride → HCID 86588256, compound
Reaction equation
NC1C=CC([C:8]2[NH:9][C:10]3[CH:16]=[CH:15][C:14](N)=[CH:13][C:11]=3[N:12]=2)=CC=1.[C:18]1([C@@H:24]2[CH2:26][C@H:25]2[C:27](Cl)=[O:28])[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>>[C:18]1([C@@H:24]2[CH2:26][C@H:25]2[C:27]([C:8]2[NH:9][C:10]3[CH:16]=[CH:15][CH:14]=[CH:13][C:11]=3[N:12]=2)=[O:28])[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1Participants
3
Procedure
Bis-trans-2-phenyl-cyclopropanecarbonyl benzimidazole was prepared by method C from 2-(4-aminophenyl)-6-amino benzimidazole (0.500 g, 2.23 mmole) and trans-2-phenyl-cyclopropanecarbonyl chloride (0.831 ml, 0.966 g, 5.35 mmole). The resulting solid was purified on silica gel (5% MeOH in CH2Cl2). HPLC showed the product was 95.5% pure.
Workup
- customThe resulting solid was purified on silica gel (5% MeOH in CH2Cl2)
Sources & evidence
- ORD record
- ord-bc4850e9a9ac486199fb354d020aea8c
- Source dataset
- uspto-grants-2005_06
- Patent number
- US06911462B2
Reaction notes
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