Sodium borohydride → HCID 18934196, compound
Reaction equation
[C:1]([NH:5][S:6]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[C:15](=[O:19])[CH:16]([F:18])[CH3:17])(=[O:8])=[O:7])([CH3:4])([CH3:3])[CH3:2].[BH4-].[Na+]>CO>[C:1]([NH:5][S:6]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[CH:15]([OH:19])[CH:16]([F:18])[CH3:17])(=[O:8])=[O:7])([CH3:3])([CH3:2])[CH3:4]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
10 g of N-t-butyl-2-(2-fluoropropionyl)benzenesulfonamide was dissolved in 100 ml of methanol, and herein 1.3 g of sodium borohydride was added in the solution at room temperature.
Sources & evidence
- ORD record
- ord-8f73d3cfc4ed45369e067d453f543df2
- Source dataset
- uspto-grants-1995_10
- Patent number
- US05461025
Reaction notes
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