Hydrochloric Acid → 7-[3-Amino-4-methylpiperidinyl]-1-cyclopropyl-1,4-dihydro-8-methoxy-4-oxo-quinoline-3-carboxylic acid hydrochloride salt
Reaction equation
[NH2:1][CH:2]1[CH:7]([CH3:8])[CH2:6][CH2:5][N:4]([C:9]2[C:18]([O:19][CH3:20])=[C:17]3[C:12]([C:13](=[O:27])[C:14]([C:24]([OH:26])=[O:25])=[CH:15][N:16]3[CH:21]3[CH2:23][CH2:22]3)=[CH:11][CH:10]=2)[CH2:3]1.[ClH:28]>C(O)C>[ClH:28].[NH2:1][CH:2]1[CH:7]([CH3:8])[CH2:6][CH2:5][N:4]([C:9]2[C:18]([O:19][CH3:20])=[C:17]3[C:12]([C:13](=[O:27])[C:14]([C:24]([OH:26])=[O:25])=[CH:15][N:16]3[CH:21]3[CH2:23][CH2:22]3)=[CH:11][CH:10]=2)[CH2:3]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A quantity of 0.20 g of 7-[3-amino-4-methylpiperidinyl]-1-cyclopropyl-1,4-dihydro-8-methoxy-4-oxo-quinoline-3-carboxylic acid is suspended in 1.0 mL of ethanol. Its pH is adjusted to 2 with hydrogen chloride to obtain the desired product after the evaporation of solvent.
Sources & evidence
- ORD record
- ord-7a114be64c2b4976b7588448a0881350
- Source dataset
- uspto-grants-2009_01
- Patent number
- US07482454B2
Reaction notes
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