HCID 86591877, compound → HCID 86591876, compound
Reaction equation
C1(C([N:6]2[C:10]3=[CH:11][N:12]=[C:13]([C:15]4[CH:16]=[N:17][C:18]([CH3:21])=[CH:19][CH:20]=4)[CH:14]=[C:9]3[C:8]([NH:22][C:23]([CH:25]3[CH2:27][CH2:26]3)=[O:24])=[N:7]2)=O)CC1>N1CCCCC1>[CH3:21][C:18]1[N:17]=[CH:16][C:15]([C:13]2[CH:14]=[C:9]3[C:8]([NH:22][C:23]([CH:25]4[CH2:27][CH2:26]4)=[O:24])=[N:7][NH:6][C:10]3=[CH:11][N:12]=2)=[CH:20][CH:19]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
Cyclopropanecarboxylic acid [1-(1-cyclopropylmethanoyl)-5-(6-methylpyridin-3-yl)-1H-pyrazolo[3,4-c]pyridin-3-yl]amide (Description 4; 196 mg, 0.542 mmol), was dissolved in piperidine (2 mL) and stirred at room temperature for 16 hours. The piperidine was removed in vacuo, and the resulting oily residue was triturated with water to give the title compound as a solid.
Workup
- customThe piperidine was removed in vacuo
- customthe resulting oily residue was triturated with water
Sources & evidence
- ORD record
- ord-f4b4516dc9374f67aa78d16ac3f3fb77
- Source dataset
- uspto-grants-2006_09
- Patent number
- US07105532B2
Reaction notes
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