Cyclohexanol → HCID 59446942, compound
Reaction equation
[CH:1]1([OH:7])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[H-].[Na+].Cl[C:11]1[N:16]=[CH:15][N:14]=[C:13]([C:17]([NH:19][C:20]2[CH:25]=[CH:24][C:23]([OH:26])=[CH:22][C:21]=2C)=[O:18])[CH:12]=1>O1CCCC1>[CH:1]1([O:7][C:11]2[N:16]=[CH:15][N:14]=[C:13]([C:17]([NH:19][C:20]3[CH:25]=[CH:24][C:23]([OH:26])=[CH:22][CH:21]=3)=[O:18])[CH:12]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Cyclohexanol (Fluka, 4.00 mL; 37.8 mmol) was treated with sodium hydride (35.0 mg; 0.80 mmol) and stirred during 10 minutes. Tetrahydrofuran (3 mL) was added, followed by 6-chloro-N-(4-hydroxy-2-methylphenyl)pyrimidine-4-carboxamide. Intermediate 7 (50.0 mg; 0.20 mmol). After 2 hours the solvents were removed in vacuo, the crude was redissolved in EtOAc. The organic phase was washed with sat. ammonium chloride and brine, dried over magnesium sulfate, filtered and evaporated in vacuo to give a residue, which was purified by column chromatography (silica) eluting with cyclohexane containing increasing amounts of EtOAc. The title compound was obtained as a white solid.
Workup
- customAfter 2 hours the solvents were removed in vacuo
- dissolutionthe crude was redissolved in EtOAc
- washThe organic phase was washed with sat. ammonium chloride and brine
- dry with materialdried over magnesium sulfate
- filtrationfiltered
- customevaporated in vacuo
- customto give a residue, which
- customwas purified by column chromatography (silica)
- washeluting with cyclohexane containing
- temperatureincreasing amounts of EtOAc
Sources & evidence
- ORD record
- ord-05abfca4e8bc444a9f5d01fe89b895a6
- Source dataset
- uspto-grants-2013_03
- Patent number
- US08399448B2
Reaction notes
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