3,3-Dimethyl-1-butanol → HCID 11952020, compound
Reaction equation
Br[C:2]1[CH:3]=[C:4]([C:9]([OH:11])=O)[CH:5]=[N:6][C:7]=1Cl.[CH3:12][C:13]([CH3:18])([CH3:17])[CH2:14][CH2:15][OH:16].[Cl:19][C:20]1[CH:25]=[CH:24][C:23](B(O)O)=[CH:22][CH:21]=1.Cl.[NH2:30][C@@H:31]1[CH2:36][CH2:35][CH2:34][CH2:33][C@H:32]1[OH:37]>>[Cl:19][C:20]1[CH:25]=[CH:24][C:23]([C:2]2[C:7]([O:16][CH2:15][CH2:14][C:13]([CH3:18])([CH3:17])[CH3:12])=[N:6][CH:5]=[C:4]([CH:3]=2)[C:9]([NH:30][C@@H:31]2[CH2:36][CH2:35][CH2:34][CH2:33][C@H:32]2[OH:37])=[O:11])=[CH:22][CH:21]=1Participants
5
Procedure
The title compound was synthesized in analogy to Example 75, using 5-bromo-6-chloro-3-pyridinecarboxylic acid, 3,3-dimethyl-1-butanol, (4-chloro-phenyl)-boronic acid and (1R,2R)-2-amino-cyclohexanol hydrochloride as starting materials to yield 5-(4-chloro-phenyl)-6-(3,3-dimethyl-butoxy)-N-((1R,2R)-2-hydroxy-cyclohexyl)-nicotinamide. MS (ISP) 431.4 (M+H)+.
Workup
- customThe title compound was synthesized in analogy to Example 75
Sources & evidence
- ORD record
- ord-186eafdc8be445a69b8df149d5015c9c
- Source dataset
- uspto-grants-2007_06
- Patent number
- US07229999B2
Reaction notes
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