Hydrochloric Acid → 1-({[2-(Benzylthio)-6-chloropyrimidin-4-yl]amino}sulfonyl)-N,N-dimethyl-D-prolinamide

HRID 424664Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 424664
[H-].[Na+].[NH2:3][S:4]([N:7]1[CH2:16][CH2:15][CH2:14][C@@H:8]1[C:9]([N:11]([CH3:13])[CH3:12])=[O:10])(=[O:6])=[O:5].[CH2:17]([S:24][C:25]1[N:30]=[C:29](NS(C)(=O)=O)[CH:28]=[C:27](NCCO)[N:26]=1)[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1.[ClH:40]>CN(C=O)C>[CH2:17]([S:24][C:25]1[N:30]=[C:29]([NH:3][S:4]([N:7]2[CH2:16][CH2:15][CH2:14][C@@H:8]2[C:9]([N:11]([CH3:13])[CH3:12])=[O:10])(=[O:6])=[O:5])[CH:28]=[C:27]([Cl:40])[N:26]=1)[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1

Komponenten

6

Versuchsvorschrift

60% Sodium hydride (0.42 g) was added to a solution of the subtitle product of step iii) (1.50 g) in DMF (20 ml) at 0° C. This mixture was stirred for 1 h and then a solution of the subtitle product of Example 19 step (1.60 g) in DMF (5 ml) was added dropwise. The mixture was allowed to reach room temperature and stirred there for 2 days. To the mixture was added aqueous hydrochloric acid (100 ml) and the resulting precipitate was filtered. This solid was then stirred with EtOAc (200 ml) and filtered to afford the subtitle compound as a solid. Yield: 2.0 g.

Aufarbeitung

  1. customto reach room temperature
  2. stirringstirred there for 2 days
  3. filtrationthe resulting precipitate was filtered
  4. stirringThis solid was then stirred with EtOAc (200 ml)
  5. filtrationfiltered

Quellen und Nachweise

ORD-Eintrag
ord-d4a4f5c0daca464e8cd7645920ff4bbf
Quelldatensatz
uspto-grants-2012_01
Patentnummer
US08106063B2

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