HCID 89963153, Verbindung → HCID 89962247, Verbindung
Reaktionsgleichung
[Cl:1][C:2]1[C:3]([O:19][C@H:20]2[CH2:25][CH2:24][CH2:23][CH2:22][C@@H:21]2[C:26]2[N:30](COCCOC)[N:29]=[CH:28][CH:27]=2)=[CH:4][C:5]([F:18])=[C:6]([S:8]([NH:11][C:12]2[CH:17]=[CH:16][N:15]=[CH:14][N:13]=2)(=[O:10])=[O:9])[CH:7]=1>Cl.CO>[Cl:1][C:2]1[C:3]([O:19][C@H:20]2[CH2:25][CH2:24][CH2:23][CH2:22][C@@H:21]2[C:26]2[NH:30][N:29]=[CH:28][CH:27]=2)=[CH:4][C:5]([F:18])=[C:6]([S:8]([NH:11][C:12]2[CH:17]=[CH:16][N:15]=[CH:14][N:13]=2)(=[O:10])=[O:9])[CH:7]=1Komponenten
4
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
A solution of the 5-chloro-2-fluoro-4-{[(1S,2R)-2-{1-[(2-methoxyethoxy)methyl]-1H-pyrazol-5-yl}cyclohexyl]oxy}-N-(pyrimidin-4-yl)benzenesulfonamide (120 mg, 0.222 mmol) prepared in Example 158d in 6 M HCl (5.0 mL) and methanol (4.0 mL) was stirred for 5 hours under heated reflux. The reaction solution was concentrated, and the residue was purified with silica gel chromatography (dichloromethane/methanol=85:15) to yield the title compound (80.0 mg, 80%) as a pale yellow solid.