4-(Dimethylamino)benzoic acid → HCID 69675008, compound
Reaction equation
[CH3:1][N:2]([CH3:12])[C:3]1[CH:11]=[CH:10][C:6]([C:7]([OH:9])=O)=[CH:5][CH:4]=1.[NH2:13][C:14]1[CH:15]=[C:16]2[NH:22][C:21]([C:23]3[CH:28]=[CH:27][C:26]([N:29]([CH3:31])[CH3:30])=[CH:25][CH:24]=3)=[N:20][C:17]2=[N:18][CH:19]=1>>[CH3:12][N:2]([CH3:1])[C:3]1[CH:4]=[CH:5][C:6]([C:7]([NH:13][C:14]2[CH:15]=[C:16]3[NH:22][C:21]([C:23]4[CH:24]=[CH:25][C:26]([N:29]([CH3:31])[CH3:30])=[CH:27][CH:28]=4)=[N:20][C:17]3=[N:18][CH:19]=2)=[O:9])=[CH:10][CH:11]=1Participants
3
Procedure
Compound 631 was prepared according to the procedure similar to that described in Scheme III from 4-dimethylaminobenzoic acid and 6-amino-2-(4-dimethylaminophenyl)-1H-imidazo[4,5-b]pyridine. [M+H]+ calcd for C23H24N6O: 401.20; found 401.07.
Sources & evidence
- ORD record
- ord-f2efb5d04653415fafd8db5372a7c635
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09144557B2
Reaction notes
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