4-[3-(4-Benzyloxy-phenyl)-1-methyl-1H-pyrazol-4-yl]-pyridine → 4-[1-Methyl-3-(4-triisopropylsilanyloxymethyl-phenyl)-1H-pyrazol-4-yl]-pyridine
Reaction equation
C(O[C:9]1[CH:14]=[CH:13][C:12]([C:15]2[C:19]([C:20]3[CH:25]=[CH:24][N:23]=[CH:22][CH:21]=3)=[CH:18][N:17]([CH3:26])[N:16]=2)=[CH:11][CH:10]=1)C1C=CC=CC=1.N1C=CC(CC(C2C=CC([CH2:42][O:43][Si:44]([CH:51]([CH3:53])[CH3:52])([CH:48]([CH3:50])[CH3:49])[CH:45]([CH3:47])[CH3:46])=CC=2)=O)=CC=1>>[CH3:26][N:17]1[CH:18]=[C:19]([C:20]2[CH:21]=[CH:22][N:23]=[CH:24][CH:25]=2)[C:15]([C:12]2[CH:11]=[CH:10][C:9]([CH2:42][O:43][Si:44]([CH:45]([CH3:47])[CH3:46])([CH:51]([CH3:53])[CH3:52])[CH:48]([CH3:50])[CH3:49])=[CH:14][CH:13]=2)=[N:16]1Participants
3
Procedure
Following the procedure for the preparation of 4-[3-(4-Benzyloxy-phenyl)-1-methyl-1H-pyrazol-4-yl]-pyridine but substituting 2-Pyridin-4-yl-1-(4-triisopropylsilanyloxymethyl-phenyl)-ethanone provided the title compound. MS: (M+H m/z=422.2).
Sources & evidence
- ORD record
- ord-222d021277a344fdb4d2a72a8bd1f33d
- Source dataset
- uspto-grants-2008_09
- Patent number
- US07429665B2
Reaction notes
Loading…