HCID 17325486, compound → HCID 178509619, compound
Reaction equation
[O:1]1[CH2:6][CH2:5][N:4]([C:7]2[CH:12]=[CH:11][C:10]([C:13]3[NH:14][C:15]4[CH:21]=[C:20]([NH2:22])[CH:19]=[CH:18][C:16]=4[N:17]=3)=[CH:9][CH:8]=2)[CH2:3][CH2:2]1.[C:23]([C:25]1[CH:30]=[CH:29][C:28]([C:31]2[NH:32][C:33]3[CH:39]=[C:38]([C:40]([O-])=[O:41])[CH:37]=[CH:36][C:34]=3[N:35]=2)=[CH:27][CH:26]=1)#[N:24]>>[C:23]([C:25]1[CH:26]=[CH:27][C:28]([C:31]2[NH:32][C:33]3[CH:39]=[C:38]([C:40]([NH:22][C:20]4[CH:19]=[CH:18][C:16]5[NH:17][C:13]([C:10]6[CH:11]=[CH:12][C:7]([N:4]7[CH2:5][CH2:6][O:1][CH2:2][CH2:3]7)=[CH:8][CH:9]=6)=[N:14][C:15]=5[CH:21]=4)=[O:41])[CH:37]=[CH:36][C:34]=3[N:35]=2)=[CH:29][CH:30]=1)#[N:24]Participants
3
Procedure
Compound 292 was prepared according to the procedure similar to that described in Scheme V from 2-(4-morpholinophenyl)-5-aminobenzimidazole and 2-(4-cyanophenyl)benzimidazole-5-carboxylate. [M+H]+ calcd for C32H25N7O2: 540.21; found: 539.97.
Sources & evidence
- ORD record
- ord-55dcfdcafdac4148871283c6bc749d57
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09144557B2
Reaction notes
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