Benzyl 3-(3-(methylsulfonamido)benzyl)-4-oxo-1-phenyl-1,3,8-triazaspiro[4.5]decane-8-carboxylate → N-(3-((4-oxo-1-phenyl-1,3,8-triazaspiro[4.5]decan-3-yl)methyl)phenyl)methanesulfonamide
Reaction equation
[CH3:1][S:2]([NH:5][C:6]1[CH:7]=[C:8]([CH:37]=[CH:38][CH:39]=1)[CH2:9][N:10]1[C:14](=[O:15])[C:13]2([CH2:20][CH2:19][N:18](C(OCC3C=CC=CC=3)=O)[CH2:17][CH2:16]2)[N:12]([C:31]2[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=2)[CH2:11]1)(=[O:4])=[O:3]>CO.[Pd]>[O:15]=[C:14]1[C:13]2([CH2:16][CH2:17][NH:18][CH2:19][CH2:20]2)[N:12]([C:31]2[CH:32]=[CH:33][CH:34]=[CH:35][CH:36]=2)[CH2:11][N:10]1[CH2:9][C:8]1[CH:7]=[C:6]([NH:5][S:2]([CH3:1])(=[O:4])=[O:3])[CH:39]=[CH:38][CH:37]=1Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of benzyl 3-(3-(methylsulfonamido)benzyl)-4-oxo-1-phenyl-1,3,8-triazaspiro[4.5]decane-8-carboxylate (0.82 g, 1.49 mmol) in methanol (15 mL), was added 10 wt % palladium on carbon (0.15 g). After stirring under hydrogen at room temperature and atmospheric pressure for 18 hours, the reaction mixture was filtered, washed with methanol, concentrated in vacuo to obtain N-(3-((4-oxo-1-phenyl-1,3,8-triazaspiro[4.5]decan-3-yl)methyl)phenyl)methanesulfonamide (0.62 g, 99%).
Workup
- filtrationthe reaction mixture was filtered
- washwashed with methanol
- concentrationconcentrated in vacuo
Sources & evidence
- ORD record
- ord-01888fbcded145148c3752270c7a7b74
- Source dataset
- uspto-grants-2014_04
- Patent number
- US08691836B2
Reaction notes
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