Hydrochloric Acid → HCID 20531187, Verbindung

HRID 1759558Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1759558
Cl[C:2]1[N:11]=[C:10]2[C:5]([C:6](=[O:19])[C:7]([C:14]([O:16][CH2:17][CH3:18])=[O:15])=[CH:8][N:9]2[CH2:12][CH3:13])=[CH:4][C:3]=1[F:20].[C:21]([CH2:24][NH:25][CH:26]1[CH2:30][CH2:29][NH:28][CH2:27]1)(=[O:23])[CH3:22].C(N(CC)CC)C.Cl>C(Cl)(Cl)Cl>[C:21]([CH2:24][NH:25][CH:26]1[CH2:30][CH2:29][N:28]([C:2]2[N:11]=[C:10]3[C:5]([C:6](=[O:19])[C:7]([C:14]([O:16][CH2:17][CH3:18])=[O:15])=[CH:8][N:9]3[CH2:12][CH3:13])=[CH:4][C:3]=2[F:20])[CH2:27]1)(=[O:23])[CH3:22]

Komponenten

6

Versuchsvorschrift

A mixture containing ethyl 7-chloro-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylate (2.99 g), 3-(N-acetylmethylamino)pyrrolidine (2.13 g), triethylamine (1.52 g), and chloroform (30 ml) was heated to reflux for 4 hours with stirring. After cooling the mixture, 5% hydrochloric acid (20 ml) was added with stirring. The chloroform layer was separated off and the solvent was evaporated. To the residue was added 20 ml of acetonitrile and the mixture was cooled. The resulting precipitate was collected and recrystallized from acetonitrile to give 3.51 g of ethyl 7-[3-(N-acetylmethylamino)-1-pyrrolidinyl]-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylate, m.p. 212°-213° C.

Aufarbeitung

  1. temperaturewas heated
  2. temperatureto reflux for 4 hours
  3. additionwas added
  4. stirringwith stirring
  5. customThe chloroform layer was separated off
  6. customthe solvent was evaporated
  7. additionTo the residue was added 20 ml of acetonitrile
  8. temperaturethe mixture was cooled
  9. customThe resulting precipitate was collected
  10. customrecrystallized from acetonitrile

Quellen und Nachweise

ORD-Eintrag
ord-130c7483f7234a46841a59ae1a09e3af
Quelldatensatz
uspto-grants-1982_07
Patentnummer
US04341784

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