Hydrochloric Acid → HCID 178524377, compound
Reaction equation
[NH:1]([C:3]1[CH:4]=[C:5]([CH:9]=[CH:10][CH:11]=1)[C:6]([OH:8])=[O:7])[NH2:2].C([O:14][C:15]([C:17]1[CH:18]=[N:19][C:20]2[C:25]([C:26]=1Cl)=[CH:24][CH:23]=[CH:22][C:21]=2[F:28])=O)C.[OH-].[Li+].Cl>C(O)CCC.O1CCCC1.O>[F:28][C:21]1[C:20]2[NH:19][CH:18]=[C:17]3[C:15](=[O:14])[N:1]([C:3]4[CH:4]=[C:5]([CH:9]=[CH:10][CH:11]=4)[C:6]([OH:8])=[O:7])[N:2]=[C:26]3[C:25]=2[CH:24]=[CH:23][CH:22]=1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
3-Hydrazinobenzoic acid (1.91 g, 0.013 mol) was added in one portion to a stirred solution of 4-chloro-8-fluoro-quinoline-3-carboxylic acid ethyl ester (2.93 g, 0.011 mol) in n-butanol (60 ml) at room temperature. The solution was heated to reflux for 16 h, cooled to room temperature and the resulting yellow solid filtered, washed with tert-butyl methyl ether and then dried. The solid was redissolved in a solution of tetrahydrofuran:water (2:1; 21 ml) and lithium hydroxide (1.27 g, 0.031 mol) was then added. After stirring at room temperature for 16 h, concentrated hydrochloric acid (3 ml) was added dropwise to the mixture to precipitate a yellow solid which was filtered and dried under vacuum to give the title compound (intermediate 3) (2.32 g, 63%) as a bright yellow solid.
Workup
- temperatureThe solution was heated
- temperatureto reflux for 16 h
- filtrationthe resulting yellow solid filtered
- washwashed with tert-butyl methyl ether
- customdried
- additionwas then added
- customto precipitate a yellow solid which
- filtrationwas filtered
- customdried under vacuum
Sources & evidence
- ORD record
- ord-866ba5d8f9af45bb90727795f570a17b
- Source dataset
- uspto-grants-2006_07
- Patent number
- US07081456B2
Reaction notes
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