Sodium Hydroxide → HCID 14839385, compound
Reaction equation
[CH2:1]([N:3]1[C:12]2[C:7](=[CH:8][C:9]([F:34])=[C:10]([N:13]3[CH2:18][CH2:17][N:16]([CH3:19])[CH:15]([C:20]4[CH:24]=[CH:23][N:22](S(C5C=CC=CC=5)(=O)=O)[CH:21]=4)[CH2:14]3)[CH:11]=2)[C:6](=[O:35])[C:5]([C:36]([OH:38])=[O:37])=[CH:4]1)[CH3:2].[OH-].[Na+]>O1CCOCC1>[CH2:1]([N:3]1[C:12]2[C:7](=[CH:8][C:9]([F:34])=[C:10]([N:13]3[CH2:18][CH2:17][N:16]([CH3:19])[CH:15]([C:20]4[CH:24]=[CH:23][NH:22][CH:21]=4)[CH2:14]3)[CH:11]=2)[C:6](=[O:35])[C:5]([C:36]([OH:38])=[O:37])=[CH:4]1)[CH3:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 538 mg of 1-ethyl-6-fluoro-1,4-dihydro-7-[4-methyl-3-[1-(phenylsulfonyl)-1H-pyrrol-3-yl]-1-piperazinyl]-4-oxo-3-quinolinecarboxylic acid, 5 ml of 1N sodium hydroxide and 15 ml of dioxane was reacted as described in Example 56, giving 290 mg of the desired product, mp 150°-152° C.
Workup
- customwas reacted
Sources & evidence
- ORD record
- ord-1c1414279c4b479187a0e2b126707858
- Source dataset
- uspto-grants-1993_05
- Patent number
- US05210193
Reaction notes
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