Sodium Bicarbonate → N-(4-(4-(Ethyl(3-cyclopropylpropyl)amino)1-hydroxybutyl)phenyl)methanesulfonamide
Reaction equation
[CH2:1]([NH:3][CH2:4][CH2:5][CH2:6][CH:7]([C:9]1[CH:14]=[CH:13][C:12]([NH:15][S:16]([CH3:19])(=[O:18])=[O:17])=[CH:11][CH:10]=1)[OH:8])[CH3:2].C(=O)(O)[O-].[Na+].Br[CH2:26][CH2:27][CH2:28][CH:29]1[CH2:31][CH2:30]1>C(#N)C>[CH2:1]([N:3]([CH2:26][CH2:27][CH2:28][CH:29]1[CH2:31][CH2:30]1)[CH2:4][CH2:5][CH2:6][CH:7]([C:9]1[CH:10]=[CH:11][C:12]([NH:15][S:16]([CH3:19])(=[O:17])=[O:18])=[CH:13][CH:14]=1)[OH:8])[CH3:2]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
According to Procedure B (Example 17, Step IV), a stirred mixture of N-[4-[4-(ethylamino)-1-hydroxybutyl]phenyl]methanesulfonamide (Example 7, Step II) and sodium bicarbonate in acetonitrile was allowed to react will 1-bromo-3-cyclopropylpropane (Step IV) to give the titled product, a compound of Formula I'. The high resolution FAB mass spectrum had (M+H)+ at m/z 369. Theory for C19H33N2O3S: 369.2212; measured: 369.2207.
Sources & evidence
- ORD record
- ord-82a0f810140c4d61890782bb0471668f
- Source dataset
- uspto-grants-1995_04
- Patent number
- US05405997
Reaction notes
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