Sodium Hydroxide → HCID 67775110, compound

HRID 2370037Notes

Reaction equation

HRID 2370037 reaction equation
[CH3:1][O:2][CH2:3][C:4]1[CH:9]=[CH:8][C:7]([NH:10][S:11]([C:14]2[CH:19]=[CH:18][C:17]([O:20][CH3:21])=[C:16]([N:22]3[CH2:27][CH2:26][N:25]([C:28](=[O:33])[C:29]([F:32])([F:31])[F:30])[CH2:24][CH2:23]3)[CH:15]=2)(=[O:13])=[O:12])=[CH:6][CH:5]=1.[OH-:34].[Na+]>>[F:30][C:29]([F:32])([F:31])[C:28]([OH:33])=[O:34].[CH3:1][O:2][CH2:3][C:4]1[CH:9]=[CH:8][C:7]([NH:10][S:11]([C:14]2[CH:19]=[CH:18][C:17]([O:20][CH3:21])=[C:16]([N:22]3[CH2:23][CH2:24][NH:25][CH2:26][CH2:27]3)[CH:15]=2)(=[O:12])=[O:13])=[CH:6][CH:5]=1

Participants

3

Reactant 2

HCID 14798Sodium HydroxideHCID 86666032HCID 86666032, compound

Product 1

HCID 67775110HCID 67775110, compound

Procedure

The product was obtained as described in Example 1 by reaction of N-(4-methoxymethyl-phenyl)-4-methoxy-3-[4-(2,2,2-trifluoro-acetyl)piperazin-1-yl]-benzenesulfonamide with aqueous sodium hydroxide.

Workup

  1. customThe product was obtained

Sources & evidence

ORD record
ord-842778271f6a4f6c86858e8b8754ef5a
Source dataset
uspto-grants-2014_04
Patent number
US08710059B2

Reaction notes

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