Potassium Carbonate → 3-amino-1-[{4-(4-methoxyphenyl)piperazin-1-yl}propanoyl]-6-N-{p-(dimethylamino)phenyl}-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridin-7-one
Reaction equation
[NH2:1][C:2]1[C:10]2[CH2:9][CH2:8][N:7]([C:11]3[CH:16]=[CH:15][C:14]([N:17]([CH3:19])[CH3:18])=[CH:13][CH:12]=3)[C:6](=[O:20])[C:5]=2[NH:4][N:3]=1.[C:21](=[O:24])([O-])[O-].[K+].[K+].ClC[CH2:29][C:30]([N:32]1[CH2:37][CH2:36][N:35]([C:38]2[CH:43]=[CH:42][C:41]([O:44][CH3:45])=[CH:40][CH:39]=2)[CH2:34][CH2:33]1)=O>>[NH2:1][C:2]1[C:10]2[CH2:9][CH2:8][N:7]([C:11]3[CH:16]=[CH:15][C:14]([N:17]([CH3:18])[CH3:19])=[CH:13][CH:12]=3)[C:6](=[O:20])[C:5]=2[N:4]([C:21](=[O:24])[CH2:29][CH2:30][N:32]2[CH2:33][CH2:34][N:35]([C:38]3[CH:43]=[CH:42][C:41]([O:44][CH3:45])=[CH:40][CH:39]=3)[CH2:36][CH2:37]2)[N:3]=1Participants
4
Reactant 3
Product 1
Procedure
A target compound (22.2 mg, 0.043 mmol, 11.1%) was yielded in the same manner as Example 1 by reacting 3-amino-6-N-(4-(dimethylamino)phenyl)-5,6-dihydro-1H-pyrazolo[3,4-c]pyridin-7(4H)-one (105 mg, 0.387 mmol) with potassium carbonate (80.1 mg, 0.580 mmol) and 3-chloro-1-{4-(4-methoxyphenyl)piperazin-1-yl}propan-1-one (120.1 mg, 0.425 mmol).
Sources & evidence
- ORD record
- ord-62a75fbc386342f880521d2f8adbb8af
- Source dataset
- uspto-grants-2013_02
- Patent number
- US08383631B2
Reaction notes
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