Sodium Methoxide → HCID 11740606, compound

HRID 1461395Notes

Reaction equation

HRID 1461395 reaction equation
C([C:3]1[N:4]([CH:27]2[CH2:29][CH2:28]2)[C:5]2[C:10]([C:11](=[O:16])[C:12]=1[C:13]([OH:15])=[O:14])=[CH:9][C:8]([F:17])=[C:7]([C:18]1[CH:23]=[C:22]([CH3:24])[N:21]=[C:20]([CH2:25]Cl)[CH:19]=1)[CH:6]=2)C.[CH3:30][O-:31].[Na+]>CO>[CH:27]1([N:4]2[C:5]3[C:10](=[CH:9][C:8]([F:17])=[C:7]([C:18]4[CH:23]=[C:22]([CH3:24])[N:21]=[C:20]([CH2:25][O:31][CH3:30])[CH:19]=4)[CH:6]=3)[C:11](=[O:16])[C:12]([C:13]([OH:15])=[O:14])=[CH:3]2)[CH2:29][CH2:28]1

Participants

4

Procedure

A solution of 1.52 g ethyl-1-cyclopropyl--7-[2-(chloromethyl)-6-methyl-4-pyridinyl]-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid (Example 18b) in 125 ml methanol was treated with 1.5 g of powdered sodium methoxide, and the reaction mixture was heated at reflux for about 16 hours. The mixture was quenched in ice containing acetic acid and extracted with methylene dichloride. The extracts were concentrated and the residue treated with water. The solid product was collected and dried (1.11 g) and was recrystallized from ethyl acetate/hexane to give 0.91 g 1-cyclopropyl-6-fluoro-7-[2-(methoxymethyl)-6-methyl-4-pyridinyl]-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid, m.p. 192°-193° C.

Workup

  1. temperaturethe reaction mixture was heated
  2. temperatureat reflux for about 16 hours
  3. customThe mixture was quenched in ice
  4. additioncontaining acetic acid
  5. extractionextracted with methylene dichloride
  6. concentrationThe extracts were concentrated
  7. additionthe residue treated with water
  8. customThe solid product was collected
  9. customdried (1.11 g)
  10. customwas recrystallized from ethyl acetate/hexane

Sources & evidence

ORD record
ord-8f8b4bc933aa4174907ebccff172c5ba
Source dataset
uspto-grants-1991_12
Patent number
US05075319

Reaction notes

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