Reaktionsgleichung
[NH2:1][C:2]1[S:3][CH:4]=[C:5]([CH2:7][C:8]([O:10][CH2:11][CH3:12])=[O:9])[N:6]=1.[CH3:13][N:14]1[C:18]([C:19]([F:22])([F:21])[F:20])=[CH:17][C:16]([C:23]2[S:24][C:25]([S:28](Cl)(=[O:30])=[O:29])=[CH:26][CH:27]=2)=[N:15]1>>[CH3:13][N:14]1[C:18]([C:19]([F:20])([F:21])[F:22])=[CH:17][C:16]([C:23]2[S:24][C:25]([S:28]([NH:1][C:2]3[S:3][CH:4]=[C:5]([CH2:7][C:8]([O:10][CH2:11][CH3:12])=[O:9])[N:6]=3)(=[O:30])=[O:29])=[CH:26][CH:27]=2)=[N:15]1Komponenten
3
Versuchsvorschrift
The title compound was prepared from ethyl 2-amino-4-thiazolylacetate and 2-[1-methyl-5-(trifluoromethyl)pyrazol-3-yl]-thiophene-5-sulfonyl chloride as described in the synthetic METHOD B giving a yellow solid with a purity of 93%. MS (electrospray, [M+H]+) m/z 481.0.
Aufarbeitung
- customgiving a yellow solid with a purity of 93%
Quellen und Nachweise
- ORD-Eintrag
- ord-af86f5c33c524254b774fe3b4a53e8eb
- Quelldatensatz
- uspto-grants-2009_11
- Patentnummer
- US07618961B2
Verknüpfte Notizen
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