1-Ethyl-1H-pyrazole-4-boronic acid, pinacol ester → 1-(2-Methoxyethyl)-1H-pyrazole-4-boronic acid, pinacol ester
Reaction equation
[CH2:1]([N:3]1[CH:7]=[C:6]([B:8]2[O:12][C:11]([CH3:14])([CH3:13])[C:10]([CH3:16])([CH3:15])[O:9]2)[CH:5]=[N:4]1)[CH3:2].[CH3:17][O:18]CCN1C=C(Br)C=N1>>[CH3:17][O:18][CH2:2][CH2:1][N:3]1[CH:7]=[C:6]([B:8]2[O:12][C:11]([CH3:14])([CH3:13])[C:10]([CH3:15])([CH3:16])[O:9]2)[CH:5]=[N:4]1Participants
3
Procedure
The title compound was prepared in the same manner as 1-ethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole, using 1-(2-methoxyethyl)-4-bromo-1H-pyrazole (see Ivachtchenko, A. V., et al J. Het. Chem. 2004, 41, 931-939).
Sources & evidence
- ORD record
- ord-035dc8cc84cd4342bdbdf653a0c4dee6
- Source dataset
- uspto-grants-2012_07
- Patent number
- US08217177B2
Reaction notes
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