3-(2,5-Dichloropyrimidin-4-yl)-1H-indole → HCID 66710098, compound
Reaction equation
Cl[C:2]1[N:7]=[C:6]([C:8]2[C:16]3[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=3)[NH:10][CH:9]=2)[C:5]([Cl:17])=[CH:4][N:3]=1.[NH2:18][C:19]1[CH:24]=[CH:23][C:22]([N:25]2[CH2:30][CH2:29][CH:28]([NH:31][CH2:32][CH2:33][OH:34])[CH2:27][CH2:26]2)=[CH:21][C:20]=1[O:35][CH3:36]>>[Cl:17][C:5]1[C:6]([C:8]2[C:16]3[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=3)[NH:10][CH:9]=2)=[N:7][C:2]([NH:18][C:19]2[CH:24]=[CH:23][C:22]([N:25]3[CH2:30][CH2:29][CH:28]([NH:31][CH2:32][CH2:33][OH:34])[CH2:27][CH2:26]3)=[CH:21][C:20]=2[O:35][CH3:36])=[N:3][CH:4]=1Participants
3
Procedure
Starting materials: 3-(2,5-dichloropyrimidin-4-yl)-1H-indole (INTERMEDIATE 2) 2-(1-(4-amino-3-methoxyphenyl)piperidin-4-ylamino)ethanol (INTERMEDIATE 31).
Sources & evidence
- ORD record
- ord-405c4dd6798840709a1f34a02a772f3b
- Source dataset
- uspto-grants-2013_06
- Patent number
- US08461170B2
Reaction notes
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