Potassium Carbonate → 3-amino-1-[{4-(4-chlorophenyl)piperazin-1-yl}propanoyl]-6-N-(p-tolyl)-4,5,6,7-tetrahydro-1-H-pyrazolo[3,4-c]pyridin-7-one

HRID 390017Notes

Reaction equation

HRID 390017 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]([CH3:17])=[CH:13][CH:12]=3)[C:6](=[O:18])[C:5]=2[NH:4][N:3]=1.[C:19](=[O:22])([O-])[O-].[K+].[K+].ClC[CH2:27][C:28]([N:30]1[CH2:35][CH2:34][N:33]([C:36]2[CH:41]=[CH:40][C:39]([Cl:42])=[CH:38][CH:37]=2)[CH2:32][CH2:31]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]([CH3:17])=[CH:13][CH:12]=3)[C:6](=[O:18])[C:5]=2[N:4]([C:19](=[O:22])[CH2:27][CH2:28][N:30]2[CH2:31][CH2:32][N:33]([C:36]3[CH:41]=[CH:40][C:39]([Cl:42])=[CH:38][CH:37]=3)[CH2:34][CH2:35]2)[N:3]=1

Participants

4

Reactant 3

HCID 11430Potassium CarbonateHCID 44100763-Chloro-1-(4-(4-chlorophenyl)piperazin-1-yl)propan-1-oneHCID 679969973-amino-5,6-dihydro-6-p-tolyl-1H-pyrazolo[3,4-c]pyridin-7(4H)-one

Product 1

HCID 679970003-amino-1-[{4-(4-chlorophenyl)piperazin-1-yl}propanoyl]-6-N-(p-tolyl)-4,5,6,7-tetrahydro-1-H-pyrazolo[3,4-c]pyridin-7-one

Procedure

A target compound (117.9 mg, 0.239 mmol, 57.5%) was yielded as white solid in the same manner as Example 1 by reacting 3-amino-5,6-dihydro-6-N-(p-tolyl)-1H-pyrazolo[3,4-c]pyridin-7(4H)-one (101 mg, 0.416 mmol) with potassium carbonate (86.2 mg, 0.624 mmol) and 3-chloro-1-{4-(4-chlorophenyl)piperazin-1-yl}propan-1-one (131.2 mg, 0.457 mmol).

Sources & evidence

ORD record
ord-fce7bd9895034c1e915651911e87158b
Source dataset
uspto-grants-2013_02
Patent number
US08383631B2

Reaction notes

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