Sulfuric Acid → HCID 24797451, compound
Reaction equation
N[C:2]1[C:10]2[C:5](=[N:6][C:7]([CH:31]([CH3:33])[CH3:32])=[CH:8][C:9]=2[C:11]2[CH:16]=[CH:15][C:14]([NH:17][C:18]([NH:20][C:21]3[CH:26]=[CH:25][CH:24]=[C:23]([C:27]([F:30])([F:29])[F:28])[CH:22]=3)=[O:19])=[CH:13][CH:12]=2)[NH:4][N:3]=1.S(=O)(=O)(O)O.N([O-])=O.[Na+]>>[CH:31]([C:7]1[N:6]=[C:5]2[NH:4][N:3]=[CH:2][C:10]2=[C:9]([C:11]2[CH:16]=[CH:15][C:14]([NH:17][C:18]([NH:20][C:21]3[CH:26]=[CH:25][CH:24]=[C:23]([C:27]([F:28])([F:29])[F:30])[CH:22]=3)=[O:19])=[CH:13][CH:12]=2)[CH:8]=1)([CH3:33])[CH3:32]Participants
4
Procedure
In analogy to GP 6, reaction of 100 mg of 1-[4-(3-Amino-6-isopropyl-1H-pyrazolo[3,4-b]pyridin-4-yl)-phenyl]-3-(3-trifluoromethyl-phenyl)-urea (0.22 mmol, 1 eq.) with 35 μL concentrated sulphuric acid and 37 mg sodium nitrite (2.5 eq.) yielded 72 mg of the desired product (74% yield).
Sources & evidence
- ORD record
- ord-44524b4f85124941bd26b0fae8d27b68
- Source dataset
- uspto-grants-2010_12
- Patent number
- US07846928B2
Reaction notes
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