Sodium Hydroxide → HCID 57334817, compound
Reaction equation
[CH3:1][O:2][CH2:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[NH:10][S:11]([C:14]1[CH:19]=[CH:18][C:17]([O:20][CH2:21][CH3:22])=[C:16]([N:23]2[CH2:28][CH2:27][N:26](C(=O)C(F)(F)F)[CH2:25][CH2:24]2)[CH:15]=1)(=[O:13])=[O:12].[OH-].[Na+]>>[CH3:1][O:2][CH2:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[NH:10][S:11]([C:14]1[CH:19]=[CH:18][C:17]([O:20][CH2:21][CH3:22])=[C:16]([N:23]2[CH2:24][CH2:25][NH:26][CH2:27][CH2:28]2)[CH:15]=1)(=[O:12])=[O:13]Participants
3
Procedure
0.074 g of the product was obtained as described in Example 1 by reaction of N-(2-methoxymethyl-phenyl)-4-ethoxy-3-[4-(2,2,2-trifluoro-acetyl)piperazin-1-yl]-benzenesulfonamide with aqueous sodium hydroxide.
Sources & evidence
- ORD record
- ord-df704e06cf7244939b1b18d05db2ec58
- Source dataset
- uspto-grants-2014_04
- Patent number
- US08710059B2
Reaction notes
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