Reaktionsgleichung
[NH2:1][CH2:2][C@H:3]1[C@@H:8]([CH3:9])[CH2:7][CH2:6][CH2:5][N:4]1[C:10]([C:12]1[N:13]=[C:14]([CH3:24])[S:15][C:16]=1[C:17]1[CH:22]=[CH:21][C:20]([F:23])=[CH:19][CH:18]=1)=[O:11].[CH2:25]([C:27]1[CH:28]=[N:29][C:30](Cl)=[N:31][CH:32]=1)[CH3:26].CCN(C(C)C)C(C)C>C(O)(C)C>[CH2:25]([C:27]1[CH:28]=[N:29][C:30]([NH:1][CH2:2][C@H:3]2[C@@H:8]([CH3:9])[CH2:7][CH2:6][CH2:5][N:4]2[C:10]([C:12]2[N:13]=[C:14]([CH3:24])[S:15][C:16]=2[C:17]2[CH:18]=[CH:19][C:20]([F:23])=[CH:21][CH:22]=2)=[O:11])=[N:31][CH:32]=1)[CH3:26]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 110 °C
Versuchsvorschrift
A mixture of rac-cis-(2-(aminomethyl)-3-methylpiperidin-1-yl)(5-(4-fluorophenyl)-2-methylthiazol-4-yl)methanone, 5-ethyl-2-chloropyrimidine, and DIPEA in isopropanol was stirred at 110° C. for 18 h. The reaction was cooled and concentrated in vacuo. The crude reaction mixture was purified by reverse-phase preparative HPLC to afford the title compound. MS (ESI) 454.02 (M+H).
Aufarbeitung
- temperatureThe reaction was cooled
- concentrationconcentrated in vacuo
- customThe crude reaction mixture
- customwas purified by reverse-phase preparative HPLC
Quellen und Nachweise
- ORD-Eintrag
- ord-aa260a00d23b419894ac9bc950ccb827
- Quelldatensatz
- uspto-grants-2016_09
- Patentnummer
- US09440982B2
Verknüpfte Notizen
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