Sodium Hydroxide → HCID 23296629, compound
Reaction equation
C([O:3][C:4]([CH2:6][CH2:7][CH2:8][N:9]1[C:13]2[CH:14]=[CH:15][C:16]([NH:18][S:19]([C:22]3[CH:23]=[CH:24][CH:25]=[C:26]4[C:31]=3[N:30]=[CH:29][CH:28]=[CH:27]4)(=[O:21])=[O:20])=[CH:17][C:12]=2[N:11]=[C:10]1[CH2:32][O:33][C:34]1[CH:39]=[CH:38][C:37]([C:40](=[NH:42])[NH2:41])=[CH:36][CH:35]=1)=[O:5])C.[OH-].[Na+]>>[OH:5][C:4]([CH2:6][CH2:7][CH2:8][N:9]1[C:13]2[CH:14]=[CH:15][C:16]([NH:18][S:19]([C:22]3[CH:23]=[CH:24][CH:25]=[C:26]4[C:31]=3[N:30]=[CH:29][CH:28]=[CH:27]4)(=[O:21])=[O:20])=[CH:17][C:12]=2[N:11]=[C:10]1[CH2:32][O:33][C:34]1[CH:35]=[CH:36][C:37]([C:40](=[NH:41])[NH2:42])=[CH:38][CH:39]=1)=[O:3]Participants
3
Procedure
Prepared analogously to Example 3 from 1-(3-ethoxycarbonylpropyl)-2-[(4-amidinophenyl)-oxymethyl]-5-(quinoline-8-sulphonylamino)-benzimidazole and sodium hydroxide solution.
Sources & evidence
- ORD record
- ord-e7cc6548923e47279fff53457aafcb6d
- Source dataset
- uspto-grants-2000_09
- Patent number
- US06121308
Reaction notes
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