Acetonitrile → 2-[(3S)-3-Aminopyrrolidin-1-yl]-6-chloro-N-[(1-hydroxycycloheptyl)methyl]-quinoline-5-carboxamide

HRID 424770Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 424770
[NH2:1][C@H:2]1[CH2:6][CH2:5][NH:4][CH2:3]1.C(#N)C.Cl[C:11]1[CH:20]=[CH:19][C:18]2[C:17]([C:21]([NH:23][CH2:24][C:25]3([OH:32])[CH2:31][CH2:30][CH2:29][CH2:28][CH2:27][CH2:26]3)=[O:22])=[C:16]([Cl:33])[CH:15]=[CH:14][C:13]=2[N:12]=1.C(=O)([O-])[O-].[K+].[K+]>O>[NH2:1][C@H:2]1[CH2:6][CH2:5][N:4]([C:11]2[CH:20]=[CH:19][C:18]3[C:17]([C:21]([NH:23][CH2:24][C:25]4([OH:32])[CH2:31][CH2:30][CH2:29][CH2:28][CH2:27][CH2:26]4)=[O:22])=[C:16]([Cl:33])[CH:15]=[CH:14][C:13]=3[N:12]=2)[CH2:3]1

Komponenten

6

Versuchsvorschrift

(S)-3 aminopyrrolidine (96 ml) and acetonitrile (300 ml) were charged to a vessel containing 2,6-Dichloro-N-((1-hydroxycycloheptyl)methyl)quinoline-5-carboxamide (300.0 g), potassium carbonate (249.0 g) and acetonitrile (2400 ml). The reaction mixture was heated under refux for 20 hours. Water (6900 ml) was charged at 20° C. to 25° C. The mixture was stirred for 95 minutes and filtered. The filter cake was washed with water (1200 ml) and acetonitrile (1200 ml). The filter cake was dried at 40° C. for 48 hours to provide the title compound as a yellow solid (283 g).

Aufarbeitung

  1. temperatureThe reaction mixture was heated under refux for 20 hours
  2. filtrationfiltered
  3. washThe filter cake was washed with water (1200 ml) and acetonitrile (1200 ml)
  4. customThe filter cake was dried at 40° C. for 48 hours

Quellen und Nachweise

ORD-Eintrag
ord-ba6ba7f8c9c04223871c75dc40294536
Quelldatensatz
uspto-grants-2012_01
Patentnummer
US08106073B2

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