Sodium Hydroxide → HCID 53788887, compound
Reaction equation
[C:1]([C:4]1[CH:9]=[CH:8][C:7]([NH:10][CH2:11][C:12]2[O:13][C:14]3[CH:21]=[C:20]([N:22]([S:29]([C:32]4[CH:33]=[CH:34][CH:35]=[C:36]5[C:41]=4[NH:40][CH2:39][CH2:38][CH2:37]5)(=[O:31])=[O:30])[CH2:23][C:24]([O:26]CC)=[O:25])[CH:19]=[CH:18][C:15]=3[C:16]=2[CH3:17])=[CH:6][CH:5]=1)(=[NH:3])[NH2:2].[OH-].[Na+]>>[C:1]([C:4]1[CH:9]=[CH:8][C:7]([NH:10][CH2:11][C:12]2[O:13][C:14]3[CH:21]=[C:20]([N:22]([S:29]([C:32]4[CH:33]=[CH:34][CH:35]=[C:36]5[C:41]=4[NH:40][CH2:39][CH2:38][CH2:37]5)(=[O:31])=[O:30])[CH2:23][C:24]([OH:26])=[O:25])[CH:19]=[CH:18][C:15]=3[C:16]=2[CH3:17])=[CH:6][CH:5]=1)(=[NH:2])[NH2:3]Participants
3
Procedure
Prepared analogously to Example 3 from 2-[N-(4-amidinophenyl)-aminomethyl]-3-methyl-6-[N-(ethoxycarbonylmethyl)-1,2,3,4-tetrahydro-quinoline-8-sulphonylamino]-benzofuran and sodium hydroxide solution.
Sources & evidence
- ORD record
- ord-f1a325b3c00d488cb195675a4abf4782
- Source dataset
- uspto-grants-2000_09
- Patent number
- US06121308
Reaction notes
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