Acetic Acid → Ethyl 5,7-dichloro-8-methoxyquinoline-3-carboxylate

HRID 1436965Notes

Reaction equation

HRID 1436965 reaction equation
[CH2:1]([O:3][C:4]([C:6]1[CH:7]=[N:8][C:9]2[C:14]([C:15]=1Cl)=[C:13]([Cl:17])[CH:12]=[C:11]([Cl:18])[C:10]=2[O:19][CH3:20])=[O:5])[CH3:2].C(O)(=O)C.C(OCC)(=O)C>O1CCOCC1.[Zn]>[CH2:1]([O:3][C:4]([C:6]1[CH:7]=[N:8][C:9]2[C:14]([CH:15]=1)=[C:13]([Cl:17])[CH:12]=[C:11]([Cl:18])[C:10]=2[O:19][CH3:20])=[O:5])[CH3:2]

Participants

6

Procedure

A suspension of zinc powder (0.70 g) was stirred at 20° C. in a solution of 4,5,7-trichloro-8-methoxy-quinoline-3-carboxylic acid ethyl ester 26 (364 mg, 1.09 mmol) and acetic acid (2.2 ml) in 1,4-dioxane (15 ml). After 20 minutes, ethyl acetate (20 ml) was added and the resultant mixture filtered through a pad of celite. The filtrate was washed with saturated aqueous sodium chloride solution (10 ml), dried (MgSO4), filtered, and the solvent removed under vacuum. The residue was chromatographed on flash silica (ethyl acetate/hexane, 1:9), yielding 130 mg (39%) of the title compound 27 as a white solid. 1H NMR (CDCl3, 400 MHz): δ 9.51 (d, J=2.0, 1 H), 9.15 (d, J=2.0, 1 H), 7.72 (s, 1H), 4.51 (q, J=7.2, 2 H), 4.18 (s, 3H), 1.47 (t, J=7.2, 3 H).

Workup

  1. filtrationthe resultant mixture filtered through a pad of celite
  2. washThe filtrate was washed with saturated aqueous sodium chloride solution (10 ml)
  3. dry with materialdried (MgSO4)
  4. filtrationfiltered
  5. customthe solvent removed under vacuum
  6. customThe residue was chromatographed on flash silica (ethyl acetate/hexane, 1:9)

Sources & evidence

ORD record
ord-0e127a599cdd4f578ea71bdd1e916dd0
Source dataset
uspto-grants-2009_11
Patent number
US07619091B2

Reaction notes

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