HCID 86722838, compound → 3-[6-(2,6-difluoro-3,5-dimethoxyphenyl)-1H-pyrazolo[4,3-c]pyridin-3-yl]-6-ethyl-5,6-dihydro-7H-pyrrolo[3,4-b]pyridin-7-one
Reaction equation
[F:1][C:2]1[C:7]([O:8][CH3:9])=[CH:6][C:5]([O:10][CH3:11])=[C:4]([F:12])[C:3]=1[C:13]1[N:18]=[CH:17][C:16]2[C:19](I)=[N:20][N:21](C3CCCCO3)[C:15]=2[CH:14]=1.[CH2:29]([N:31]1[CH2:39][C:38]2[C:33](=[N:34][CH:35]=[C:36](B(O)O)[CH:37]=2)[C:32]1=[O:43])[CH3:30]>>[F:12][C:4]1[C:5]([O:10][CH3:11])=[CH:6][C:7]([O:8][CH3:9])=[C:2]([F:1])[C:3]=1[C:13]1[N:18]=[CH:17][C:16]2[C:19]([C:36]3[CH:37]=[C:38]4[CH2:39][N:31]([CH2:29][CH3:30])[C:32](=[O:43])[C:33]4=[N:34][CH:35]=3)=[N:20][NH:21][C:15]=2[CH:14]=1Participants
3
Procedure
This compound was prepared by using procedures analogous to those described for the synthesis of Example 52, Step 8 starting from 6-(2,6-difluoro-3,5-dimethoxyphenyl)-3-iodo-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazolo[4,3-c]pyridine and (6-ethyl-7-oxo-6,7-dihydro-5H-pyrrolo[3,4-b]pyridin-3-yl)boronic acid. LCMS (M+H)+=452.1.
Workup
- customThis compound was prepared
Sources & evidence
- ORD record
- ord-3646bdd29e1b40afb14029588d253b26
- Source dataset
- uspto-grants-2016_02
- Patent number
- US09266892B2
Reaction notes
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