4-(Dimethylamino)benzoic acid → HCID 69675392, compound
Reaction equation
[NH2:1][C:2]1[CH:10]=[C:9]2[C:5]([C:6]([C:20]3[CH:25]=[CH:24][C:23]([NH2:26])=[CH:22][CH:21]=3)=[CH:7][N:8]2[S:11]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)(=[O:13])=[O:12])=[CH:4][CH:3]=1.[CH3:27][N:28]([CH3:38])[C:29]1[CH:37]=[CH:36][C:32]([C:33](O)=[O:34])=[CH:31][CH:30]=1>>[CH3:27][N:28]([CH3:38])[C:29]1[CH:37]=[CH:36][C:32]([C:33]([NH:26][C:23]2[CH:22]=[CH:21][C:20]([C:6]3[C:5]4[C:9](=[CH:10][C:2]([NH:1][C:33](=[O:34])[C:32]5[CH:36]=[CH:37][C:29]([N:28]([CH3:38])[CH3:27])=[CH:30][CH:31]=5)=[CH:3][CH:4]=4)[N:8]([S:11]([C:14]4[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=4)(=[O:13])=[O:12])[CH:7]=3)=[CH:25][CH:24]=2)=[O:34])=[CH:31][CH:30]=1Participants
3
Procedure
Compound 991 was prepared according to the procedure described in Scheme IV from 6-amino-3-(4-aminophenyl)-1-(phenylsulfonyl)indole and 4-dimethylaminobenzoic acid. [M+H]+ calcd for C38H35N5O4S: 658.31; found: 658.19.
Sources & evidence
- ORD record
- ord-77c7f15e369c4f78952fa03c24b163a5
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09144557B2
Reaction notes
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