Hydrochloric Acid → HCID 178524377, compound

HRID 1793391Notes

Reaction equation

HRID 1793391 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]=1

Participants

7

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

  1. temperatureThe solution was heated
  2. temperatureto reflux for 16 h
  3. filtrationthe resulting yellow solid filtered
  4. washwashed with tert-butyl methyl ether
  5. customdried
  6. additionwas then added
  7. customto precipitate a yellow solid which
  8. filtrationwas filtered
  9. customdried under vacuum

Sources & evidence

ORD record
ord-866ba5d8f9af45bb90727795f570a17b
Source dataset
uspto-grants-2006_07
Patent number
US07081456B2

Reaction notes

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