tert-Butyl 3-{[5-chloro-4-(3-chloro-5-cyanophenoxy)-1H-1,2,3-benzotriazol-1-yl]methyl}-1H-pyrazolo[3,4-b]pyridine-1-carboxylate → HCID 178509924, compound
Reaction equation
[Cl:1][C:2]1[CH:27]=[CH:26][C:5]2[N:6]([CH2:9][C:10]3[C:18]4[C:13](=[N:14][CH:15]=[CH:16][CH:17]=4)[N:12](C(OC(C)(C)C)=O)[N:11]=3)[N:7]=[N:8][C:4]=2[C:3]=1[O:28][C:29]1[CH:34]=[C:33]([C:35]#[N:36])[CH:32]=[C:31]([Cl:37])[CH:30]=1>C(O)(C(F)(F)F)=O>[Cl:37][C:31]1[CH:32]=[C:33]([CH:34]=[C:29]([O:28][C:3]2[C:4]3[N:8]=[N:7][N:6]([CH2:9][C:10]4[C:18]5[C:13](=[N:14][CH:15]=[CH:16][CH:17]=5)[NH:12][N:11]=4)[C:5]=3[CH:26]=[CH:27][C:2]=2[Cl:1])[CH:30]=1)[C:35]#[N:36]Participants
3
Procedure
tert-Butyl 3-{[5-chloro-4-(3-chloro-5-cyanophenoxy)-1H-1,2,3-benzotriazol-1-yl]methyl}-1H-pyrazolo[3,4-b]pyridine-1-carboxylate (0.001 g, 1.86 μmol) was dissolved in TFA (2 mL) at room temperature. After 5 minutes, the solvent was evaporated in vacuo to afford the title product.
Workup
- customthe solvent was evaporated in vacuo
Sources & evidence
- ORD record
- ord-d4b08d252c634facbee45831f0640f27
- Source dataset
- uspto-grants-2010_08
- Patent number
- US07781454B2
Reaction notes
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