HCID 23296430, compound → HCID 23296641, compound
Reaction equation
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([CH2:9][C:10]([N:12]2[CH2:21][CH2:20][C:19]3[C:14](=[CH:15][C:16]([NH:22][S:23]([C:26]4[CH:27]=[CH:28][CH:29]=[C:30]5[C:35]=4[N:34]=[CH:33][CH:32]=[CH:31]5)(=[O:25])=[O:24])=[CH:17][CH:18]=3)[CH2:13]2)=[O:11])=[CH:5][CH:4]=1)#[N:2].[ClH:36].C(=O)([O-])[O-].[NH4+:41].[NH4+]>C(O)C>[ClH:36].[C:1]([C:3]1[CH:8]=[CH:7][C:6]([CH2:9][C:10]([N:12]2[CH2:21][CH2:20][C:19]3[C:14](=[CH:15][C:16]([NH:22][S:23]([C:26]4[CH:27]=[CH:28][CH:29]=[C:30]5[C:35]=4[N:34]=[CH:33][CH:32]=[CH:31]5)(=[O:25])=[O:24])=[CH:17][CH:18]=3)[CH2:13]2)=[O:11])=[CH:5][CH:4]=1)(=[NH:41])[NH2:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Prepared analogously to Example 1e from 2-[(4-cyanophenyl)-acetyl]-7-(quinoline-8-sulphonylamino)-1,2,3,4-tetrahydro-isoquinoline and hydrochloric acid/ammonium carbonate in ethanol.
Sources & evidence
- ORD record
- ord-3c41d5a0dfca46b38c39a154a35d1c21
- Source dataset
- uspto-grants-2000_09
- Patent number
- US06121308
Reaction notes
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