Reaction #335643

ord-0e7d464895b94570a0d7b9c91f1bdccd

Reaction equation

OCC1CNCCN1
2-hydroxymethylpiperazine
CCn1cc(C(=O)O)c(=O)c2cc(F)c(Cl)cc21
7-chloro-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid
CCn1cc(C(=O)O)c(=O)c2cc(F)c(N3CCNC(CO)C3)cc21.Cl
1-Ethyl-6-fluoro-1,4-dihydro-7[3-(hydroxymethyl)-1-piperazinyl]-4-oxo-3-quinolinecarboxylic acid, hydrochloride

Solvents

Conditions

Temperature
130°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    OtherThe solvent was removed
  2. 2
    workup.ADDITIONadded to a column of flash grade silica gel
  3. 3
    WashThe column was eluted with methanol:water (95:5)
  4. 4
    OtherThe product fraction was collected
  5. 5
    workup.DISSOLUTIONdissolved in methanoldichloromethane

Procedure

A mixture of 2 g of 2-hydroxymethylpiperazine, 1 g of 7-chloro-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid and 8 ml of pyridine was heated at 130° C. in a sealed bottle, under argon, overnight. The solvent was removed and the residue adsorbed onto silica gel, then added to a column of flash grade silica gel. The column was eluted with methanol:water (95:5). The product fraction was collected, dissolved in methanoldichloromethane and converted to the hydrochloride salt, mp>275° C.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05210193uspto-grants-1993_05