Hydrochloric Acid → 6-(4-{[(3,4-dichloro-5-methyl-1H-pyrrol-2-yl)carbonyl]amino}piperidin-1-yl)-2-morpholin-4-ylpyrimidine-4-carboxylic acid
Reaktionsgleichung
[Cl:1][C:2]1[C:6]([Cl:7])=[C:5]([CH3:8])[NH:4][C:3]=1[C:9]([NH:11][CH:12]1[CH2:17][CH2:16][N:15]([C:18]2[N:23]=[C:22]([N:24]3[CH2:29][CH2:28][O:27][CH2:26][CH2:25]3)[N:21]=[C:20]([C:30]([O:32]C)=[O:31])[CH:19]=2)[CH2:14][CH2:13]1)=[O:10].[OH-].[Li+].Cl>CO>[Cl:1][C:2]1[C:6]([Cl:7])=[C:5]([CH3:8])[NH:4][C:3]=1[C:9]([NH:11][CH:12]1[CH2:13][CH2:14][N:15]([C:18]2[N:23]=[C:22]([N:24]3[CH2:25][CH2:26][O:27][CH2:28][CH2:29]3)[N:21]=[C:20]([C:30]([OH:32])=[O:31])[CH:19]=2)[CH2:16][CH2:17]1)=[O:10]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Methyl 6-(4-{[(3,4-dichloro-5-methyl-1H-pyrrol-2-yl)carbonyl]amino}piperidin-1-yl)-2-morpholin-4-ylpyrimidine-4-carboxylate (Example 9, 224 mg, 0.45 mmol) was dissolved in MeOH (5 ml). 2 N lithium hydroxide (2 ml) was added and the reaction was stirred at room temperature for 3 h. The mixture was acidified with 1 N HCl and was extracted with EtOAc (3×50 ml), dried over Na2SO4 and concentrated in vacuo to provide 200 mg of the title compound.
Aufarbeitung
- extractionwas extracted with EtOAc (3×50 ml)
- dry with materialdried over Na2SO4
- concentrationconcentrated in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-c0914202334c47b39cf838662b0e27f3
- Quelldatensatz
- uspto-grants-2010_05
- Patentnummer
- US07709503B2
Notizen zur Reaktion
Wird geladen…