Pyridine → Methyl 4-(3-chloro-4-[(phenoxycarbonyl)amino]phenoxy}-7-(2-methoxyethoxy)-6-quinolinecarboxylate

HRID 1433515Notes

Reaction equation

HRID 1433515 reaction equation
[NH2:1][C:2]1[CH:27]=[CH:26][C:5]([O:6][C:7]2[C:16]3[C:11](=[CH:12][C:13]([O:21][CH2:22][CH2:23][O:24][CH3:25])=[C:14]([C:17]([O:19][CH3:20])=[O:18])[CH:15]=3)[N:10]=[CH:9][CH:8]=2)=[CH:4][C:3]=1[Cl:28].N1C=CC=CC=1.O1CCCC1.Cl[C:41]([O:43][C:44]1[CH:49]=[CH:48][CH:47]=[CH:46][CH:45]=1)=[O:42]>O>[Cl:28][C:3]1[CH:4]=[C:5]([CH:26]=[CH:27][C:2]=1[NH:1][C:41]([O:43][C:44]1[CH:49]=[CH:48][CH:47]=[CH:46][CH:45]=1)=[O:42])[O:6][C:7]1[C:16]2[C:11](=[CH:12][C:13]([O:21][CH2:22][CH2:23][O:24][CH3:25])=[C:14]([C:17]([O:19][CH3:20])=[O:18])[CH:15]=2)[N:10]=[CH:9][CH:8]=1

Participants

6

Procedure

Methyl 4-(4-amino-3-chlorophenoxy)-7-(2-methoxyethoxy)-6-quinolinecarboxylate (3.2 g), pyridine (0.71 ml) and tetrahydrofuran (50 ml) were stirred while cooling on ice, and then 1.1 ml of phenyl chloroformate was added dropwise. After 40 minutes, 0.8 ml of pyridine and 1.1 ml of phenyl chloroformate were added and the mixture was stirred for an additional 10 minutes. Water was added, extraction was performed with ethyl acetate, and the extract solution was passed through a glass filter coated with silica gel. The silica gel was washed with ethyl acetate, the solvent was distilled off under reduced pressure, hexane and ethyl acetate were added to the residue and the solid was filtered out to obtain 3.2 g of a faint red solid.

Workup

  1. temperaturewhile cooling on ice
  2. extractionextraction
  3. filtrationfilter
  4. washThe silica gel was washed with ethyl acetate
  5. distillationthe solvent was distilled off under reduced pressure, hexane and ethyl acetate
  6. additionwere added to the residue
  7. filtrationthe solid was filtered out

Sources & evidence

ORD record
ord-9616e10c3cd741619fd6734874697eef
Source dataset
uspto-grants-2009_11
Patent number
US07612092B2

Reaction notes

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