Sodium Hydroxide → HCID 23296440, compound
Reaction equation
[CH3:1][N:2]1[C:10]2[C:5](=[CH:6][C:7]([N:11]([S:18]([C:21]3[CH:22]=[CH:23][CH:24]=[C:25]4[C:30]=3[N:29]=[CH:28][CH:27]=[CH:26]4)(=[O:20])=[O:19])[CH2:12][C:13]([O:15]CC)=[O:14])=[CH:8][CH:9]=2)[CH:4]=[C:3]1[CH2:31][CH2:32][C:33]1[CH:38]=[CH:37][C:36]([C:39](=[NH:41])[NH2:40])=[CH:35][CH:34]=1.[OH-].[Na+]>>[CH3:1][N:2]1[C:10]2[C:5](=[CH:6][C:7]([N:11]([S:18]([C:21]3[CH:22]=[CH:23][CH:24]=[C:25]4[C:30]=3[N:29]=[CH:28][CH:27]=[CH:26]4)(=[O:20])=[O:19])[CH2:12][C:13]([OH:15])=[O:14])=[CH:8][CH:9]=2)[CH:4]=[C:3]1[CH2:31][CH2:32][C:33]1[CH:34]=[CH:35][C:36]([C:39](=[NH:40])[NH2:41])=[CH:37][CH:38]=1Participants
3
Procedure
Prepared analogously to Example 3 from 1-methyl-2-[2-(4-amidinophenyl)-ethyl]-5-[N-(ethoxycarbonylmethyl)-quinoline-8-sul-phonylamino]-indole and sodium hydroxide solution.
Sources & evidence
- ORD record
- ord-0d9a1d4c63274b06be9195dbccc71a64
- Source dataset
- uspto-grants-2000_09
- Patent number
- US06121308
Reaction notes
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