HCID 67112380, compound → HCID 178509620, compound

HRID 2284176Notes

Reaction equation

HRID 2284176 reaction equation
[OH:1][CH2:2][CH2:3][N:4]([CH2:21][CH2:22][OH:23])[C:5]1[CH:10]=[CH:9][C:8]([C:11]2[NH:12][C:13]3[CH:19]=[C:18]([NH2:20])[CH:17]=[CH:16][C:14]=3[N:15]=2)=[CH:7][CH:6]=1.[C:24]([C:26]1[CH:31]=[CH:30][C:29]([C:32]2[NH:33][C:34]3[CH:40]=[C:39]([C:41]([O-])=[O:42])[CH:38]=[CH:37][C:35]=3[N:36]=2)=[CH:28][CH:27]=1)#[N:25]>>[OH:1][CH2:2][CH2:3][N:4]([CH2:21][CH2:22][OH:23])[C:5]1[CH:10]=[CH:9][C:8]([C:11]2[NH:15][C:14]3[CH:16]=[CH:17][C:18]([NH:20][C:41]([C:39]4[CH:38]=[CH:37][C:35]5[N:36]=[C:32]([C:29]6[CH:28]=[CH:27][C:26]([C:24]#[N:25])=[CH:31][CH:30]=6)[NH:33][C:34]=5[CH:40]=4)=[O:42])=[CH:19][C:13]=3[N:12]=2)=[CH:7][CH:6]=1

Participants

3

Procedure

Compound 293 was prepared according to the procedure similar to that described in Scheme V from 2-(4-(bis(2-hydroxyethyl)amino)phenyl)-5-aminobenzimidazole and 2-(4-cyanophenyl)benzimidazole-5-carboxylate. [M+H]+ calcd for C32H25N7O3: 558.22; found: 557.99.

Sources & evidence

ORD record
ord-99d40cf3760042e68c1ca7e91ca1ffaa
Source dataset
uspto-grants-2015_09
Patent number
US09144557B2

Reaction notes

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