1,8-Diazabicyclo(5.4.0)undec-7-ene → 1-Cyclopropyl-7-(1,4-diazabicyclo[3.2.1]octan-4-yl)-6,8-difluoro-4-oxo-quinoline-3-carboxylic acid

HRID 1589575Notes

Reaction equation

HRID 1589575 reaction equation
[CH:1]1([N:4]2[C:13]3[C:8](=[CH:9][C:10]([F:16])=[C:11](F)[C:12]=3[F:14])[C:7](=[O:17])[C:6]([C:18]([OH:20])=[O:19])=[CH:5]2)[CH2:3][CH2:2]1.[N:21]12[CH2:28][CH:25]([CH2:26][CH2:27]1)[NH:24][CH2:23][CH2:22]2.N12CCCN=C1CCCCC2>C(#N)C>[CH:1]1([N:4]2[C:13]3[C:8](=[CH:9][C:10]([F:16])=[C:11]([N:24]4[CH:25]5[CH2:28][N:21]([CH2:27][CH2:26]5)[CH2:22][CH2:23]4)[C:12]=3[F:14])[C:7](=[O:17])[C:6]([C:18]([OH:20])=[O:19])=[CH:5]2)[CH2:2][CH2:3]1

Participants

5

Procedure

A mixture of 1.14 g (4 mmol) 1-cyclopropyl-6,7,8-trifluoro-4-oxo-1,4-dihydro-3-quinolinecarboxylic acid, 0.62 g (5.5 mmol) 1,4-diazabicyclo[3.2.1]octane and 0.40 g (4 mmol) 1,8-diazabicyclo[5.4.0]undec-7-ene in 20 ml acetonitrile was refluxed 6.5 hours. After cooling to room temperature the solid product was filtered, suspended in 10 ml hot ethanol, cooled, and filtered to afford 0.55 g of 1-cyclopropyl-7-(1,4-diazabicyclo[3.2.1]octan-4-yl)-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid, mp 280° C. (dec).

Workup

  1. temperaturewas refluxed 6.5 hours
  2. filtrationwas filtered
  3. temperaturecooled
  4. filtrationfiltered

Sources & evidence

ORD record
ord-52ae4cdae5ea47828f7d4a37a08990f2
Source dataset
uspto-grants-1986_02
Patent number
US04571396

Reaction notes

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