Sodium Bicarbonate → HCID 10668837, compound

HRID 1654309Notes

Reaction equation

HRID 1654309 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][CH2:29][C:30]([F:33])([CH3:32])[CH3:31]>C(#N)C>[CH2:1]([N:3]([CH2:26][CH2:27][CH2:28][CH2:29][C:30]([F:33])([CH3:32])[CH3:31])[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

HCID 516892Sodium BicarbonateHCID 10584068HCID 10584068, compoundHCID 10779588N-(4-(4-(ethylamino)-1-hydroxybutyl)phenyl)methanesulfonamide

Product 1

HCID 10668837HCID 10668837, compound

Reagents, catalysts & solvents 1

HCID 6342AcetonitrileSolvent

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 with 1-bromo-5-fluoro-5-methylhexane (Step III) to give the titled product, a compound of Formula I'. The high resolution mass spectrum had M+ at m/z 402. Theory for C20H35FN2O3S: 402.2352; measured: 402.2350.

Sources & evidence

ORD record
ord-8b55c4142e1444f4a384376c2ea9a9f4
Source dataset
uspto-grants-1995_04
Patent number
US05405997

Reaction notes

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