Benzoic acid, 3-(chlorosulfonyl)- → HCID 24852121, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([NH2:19])[CH:5]=[N:6][C:7]=1[O:8][C:9]1[N:10]=[CH:11][C:12]2[C:17]([CH:18]=1)=[CH:16][CH:15]=[CH:14][CH:13]=2.Cl[S:21]([C:24]1[CH:25]=[C:26]([CH:30]=[CH:31][CH:32]=1)[C:27]([OH:29])=[O:28])(=[O:23])=[O:22]>>[Cl:1][C:2]1[CH:3]=[C:4]([NH:19][S:21]([C:24]2[CH:25]=[C:26]([CH:30]=[CH:31][CH:32]=2)[C:27]([OH:29])=[O:28])(=[O:23])=[O:22])[CH:5]=[N:6][C:7]=1[O:8][C:9]1[N:10]=[CH:11][C:12]2[C:17]([CH:18]=1)=[CH:16][CH:15]=[CH:14][CH:13]=2Participants
3
Procedure
The title compound was prepared by reacting 5-chloro-6-(isoquinolin-3-yloxy)pyridin-3-amine (obtained as per procedure described in preparation 2) and 3-(chlorosulfonyl)benzoic acid.
Sources & evidence
- ORD record
- ord-0428ab5294a944a9b0a9be64b1e7086d
- Source dataset
- uspto-grants-2012_09
- Patent number
- US08269010B2
Reaction notes
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