反应详情

A 322 mg (0.89 mmol) portion of (3R)-1-benzyloxycarbonyl-3-(1-tert-butoxycarbonylaminocyclopropyl)pyrrolidine was dissolved in 10 ml of methanol to which was subsequently added 100 mg of 5% palladium-carbon to carry out 2 hours of hydrogenation under normal pressure with warming by an infrared lamp. After completion of the reaction, 5% palladium-carbon was removed by filtration and methanol was evaporated. The resulting residue was dissolved in 5 ml of acetonitrile to which were subsequently added 0.5 ml of triethylamine and 113 mg (0.4 mmol) of 6,7-difluoro-[(1R,2S)-2-fluorocyclopropyl]-1,4-dihydro-4-oxoquinoline-3-carboxylic acid, followed by 18 hours of heating under reflux. After completion of the reaction, the reaction solution was spontaneously cooled to collect the thus formed crystals by filtration. With cooling in an ice bath, to the thus obtained crystals was added dropwise 5 ml of concentrated hydrochloric acid, followed by 30 minutes of stirring at the same temperature. After completion of the reaction, the reaction solution was adjusted to pH 12 with sodium hydroxide aqueous solution and then to pH 7.4 with hydrochloric acid, followed by extraction with chloroform (50 ml×3). The organic layers were combined and dried on sodium sulfate, and then the solvent was evaporated. Thereafter, the resulting residue was recrystallized from liquid ammonia-ethanol to yield 120 mg (77%) of the title compound.

1. temperaturewith warming by an infrared lamp
2. customwas removed by filtration and methanol
3. customwas evaporated
4. dissolutionThe resulting residue was dissolved in 5 ml of acetonitrile to which
5. waitfollowed by 18 hours
6. temperatureof heating
7. temperatureunder reflux
8. customAfter completion of the reaction
9. temperaturethe reaction solution was spontaneously cooled
10. customto collect the thus formed crystals
11. filtrationby filtration
12. temperatureWith cooling in an ice bath, to the thus obtained crystals
13. additionwas added dropwise 5 ml of concentrated hydrochloric acid
14. waitfollowed by 30 minutes
15. customAfter completion of the reaction
16. extractionto pH 7.4 with hydrochloric acid, followed by extraction with chloroform (50 ml×3)
17. customdried on sodium sulfate
18. customthe solvent was evaporated
19. customThereafter, the resulting residue was recrystallized from liquid ammonia-ethanol