Reaction equation
BrC[C:3]1[C:11]2[N:10]=[CH:9][N:8]([C:12](OC(C)(C)C)=O)[C:7]=2[CH:6]=[CH:5][CH:4]=1.[CH3:19][N:20]([CH:22](C(OCC)=O)[C:23](OCC)=O)[CH3:21].C(N(C(C(OCC)=O)[C:41](OCC)=[O:42])CCC)CC>>[CH3:41][O:42][C:5]1[CH:4]=[CH:3][C:11]2[N:10]=[CH:9][N:8]3[C:7]=2[C:6]=1[CH2:23][CH:22]([N:20]([CH3:21])[CH3:19])[CH2:12]3Participants
4
Procedure
This compound was prepared by following the procedure of Example 18, but substituting t-butyl 4-(bromomethyl)-5-methoxy-1H-benzimidazole-1-carboxylate for t-butyl 4-(bromomethyl)-1H-benzimidazole-1-carboxylate and diethyl (dimethylamino)malonate for diethyl (dipropylamino)malonate.
Workup
- customThis compound was prepared
Sources & evidence
- ORD record
- ord-4915559f40824c8fa946c0507699cd4a
- Source dataset
- uspto-grants-1993_12
- Patent number
- US05273975
Linked notes
Loading…