4-Bromo-1-(1-methylethyl)-1H-imidazole → HCID 23571073, compound
Reaction equation
Br[C:2]1[N:3]=[CH:4][N:5]([CH:7]([CH3:9])[CH3:8])[CH:6]=1.CC1(C)C(C)(C)OB([C:18]2[CH:19]=[CH:20][C:21]3[CH2:28][C@H:27]4[C@:29]5([CH2:33][N:32]([CH2:34][C:35]([F:38])([F:37])[F:36])[S:31](=[O:40])(=[O:39])[NH:30]5)[C@H:24]([CH2:25][CH2:26]4)[CH2:23][C:22]=3[CH:41]=2)O1>>[CH:7]([N:5]1[CH:6]=[C:2]([C:18]2[CH:19]=[CH:20][C:21]3[CH2:28][C@H:27]4[C@:29]5([CH2:33][N:32]([CH2:34][C:35]([F:38])([F:37])[F:36])[S:31](=[O:39])(=[O:40])[NH:30]5)[C@H:24]([CH2:25][CH2:26]4)[CH2:23][C:22]=3[CH:41]=2)[N:3]=[CH:4]1)([CH3:9])[CH3:8]Participants
3
Reactant 2
Product 1
Procedure
Prepared from 4-bromo-1-isopropyl-1H-imidazole (Step 1) and homochiral boronate from Example 24 Step 1 by the procedure described for Example 76 Step 2.
Sources & evidence
- ORD record
- ord-a7e4cb84393e42a2a709d66b0b5f133f
- Source dataset
- uspto-grants-2006_05
- Patent number
- US07041689B2
Reaction notes
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