3,5-Bis(trifluoromethyl)benzaldehyde → N-(5-((1R,2S)-2-(3,5-Bis(trifluoromethyl)benzylamino)-1-hydroxypropyl)-2-hydroxyphenyl)methanesulfonamide
Reaction equation
[NH2:1][C@@H:2]([CH3:17])[C@@H:3]([C:5]1[CH:6]=[CH:7][C:8]([OH:16])=[C:9]([NH:11][S:12]([CH3:15])(=[O:14])=[O:13])[CH:10]=1)[OH:4].[F:18][C:19]([F:33])([F:32])[C:20]1[CH:21]=[C:22]([CH:25]=[C:26]([C:28]([F:31])([F:30])[F:29])[CH:27]=1)[CH:23]=O>CO>[F:18][C:19]([F:32])([F:33])[C:20]1[CH:21]=[C:22]([CH:25]=[C:26]([C:28]([F:31])([F:29])[F:30])[CH:27]=1)[CH2:23][NH:1][C@@H:2]([CH3:17])[C@@H:3]([C:5]1[CH:6]=[CH:7][C:8]([OH:16])=[C:9]([NH:11][S:12]([CH3:15])(=[O:14])=[O:13])[CH:10]=1)[OH:4]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Borane-pyridine complex (130 μL, 1.24 mmol) was added to a methanol solution (4 mL) of an amine (3) (107 mg, 0.41 mmol), 3,5-bis(trifluoromethyl)benzaldehyde (90 μL, 0.54 mmol) at 40° C. and the mixture was stirred for 1.5 hours. The reaction mixture was allowed to cool to room temperature and extracted after addition of water with a mixed solvent (ethyl acetate: methanol=10:1), and the organic layer was washed with saturated aqueous sodium chloride solution. The organic layer was dried and concentrated, and the crude product obtained was purified by amine silica gel column chromatography (eluant:chloroform:methanol=7:1), to give a desired amine (5) as a white solid (132 mg, yield: 66%).
Workup
- extractionextracted
- additionafter addition of water with a mixed solvent (ethyl acetate: methanol=10:1)
- washthe organic layer was washed with saturated aqueous sodium chloride solution
- customThe organic layer was dried
- concentrationconcentrated
- customthe crude product obtained
- customwas purified by amine silica gel column chromatography (eluant:chloroform:methanol=7:1)
Sources & evidence
- ORD record
- ord-2a2b4274fad7474cb8f1319a1e4a7c3f
- Source dataset
- uspto-grants-2012_06
- Patent number
- US08198330B2
Reaction notes
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