Triethylamine → 5-Amino-7-(3-amino-1-pyrrolidinyl)-8-chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic Acid

HRID 620891Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 620891
[NH2:1][C:2]1[C:11]([F:12])=[C:10](F)[C:9]([Cl:14])=[C:8]2[C:3]=1[C:4](=[O:21])[C:5]([C:18]([OH:20])=[O:19])=[CH:6][N:7]2[CH:15]1[CH2:17][CH2:16]1.C(OC([NH:29][CH:30]1[CH2:34][CH2:33][NH:32][CH2:31]1)=O)(C)(C)C.C(N(CC)CC)C>C(#N)C>[NH2:1][C:2]1[C:11]([F:12])=[C:10]([N:32]2[CH2:33][CH2:34][CH:30]([NH2:29])[CH2:31]2)[C:9]([Cl:14])=[C:8]2[C:3]=1[C:4](=[O:21])[C:5]([C:18]([OH:20])=[O:19])=[CH:6][N:7]2[CH:15]1[CH2:17][CH2:16]1

Komponenten

5

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

To 1.57 g (5 mmol) of 5-amino-8-chloro-1-cyclo- propyl-6,7-difluoro-1,4-dihydro-4-oxo-3-quinoline carboxylic acid in 20 ml of acetonitrile was added 0.93 g (5 mmol) of 3-[(t-butoxycarbonyl)amino]pyrrolidine and 1.0 g (10 mmol) of triethylamine. The mixture was refluxed for three hours, cooled, and filtered. The solids were washed with acetonitrile and ether, then dissolved in 10 ml of acetic acid and 2 ml of 3 N hydrochloric acid. The mixture was heated at 100° C. for four hours, concentrated, and triturated with 2-propanol. The solid that formed was filtered and washed with ether to give 1.2 g of the title compound.

Aufarbeitung

  1. temperatureThe mixture was refluxed for three hours
  2. temperaturecooled
  3. filtrationfiltered
  4. washThe solids were washed with acetonitrile and ether
  5. dissolutiondissolved in 10 ml of acetic acid
  6. concentrationconcentrated
  7. customtriturated with 2-propanol
  8. customThe solid that formed
  9. filtrationwas filtered
  10. washwashed with ether

Quellen und Nachweise

ORD-Eintrag
ord-6b0acb7de82d456b80610d70ca5a8278
Quelldatensatz
uspto-grants-1989_04
Patentnummer
US04822801

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