Hydrochloric Acid → 2-(Pyridin-2-yl)quinoline-4-carboxylic acid
Reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7]1(C([O-])=O)[CH:16]=[C:15]([C:17]([OH:19])=[O:18])[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[NH:8]1.[Na+].Cl>>[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7]1[CH:16]=[C:15]([C:17]([OH:19])=[O:18])[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[N:8]=1Participants
3
Procedure
The free acid is prepared by neutralizing an aqueous solution of the sodium 2-(2-pyridyl)-4-carboxyquinoline carboxylate 3 with 10% HCl. The acid is somewhat soluble in acidic solution, and care should be taken not to overacidify; a pH of 7 is optimum. The solid is filtered, washed with 40 mL of acetone and allowed to air dry.
Workup
- customThe free acid is prepared
- filtrationThe solid is filtered
- washwashed with 40 mL of acetone
- customto air dry
Sources & evidence
- ORD record
- ord-6555d9c071b74344aab1a666d2ab3e89
- Source dataset
- uspto-grants-1999_02
- Patent number
- US05874587
Reaction notes
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