3-Chloro-2-methylbenzenesulfonyl chloride → 3-Chloro-N-(4-isopropyl-1,3-thiazol-2-yl)-2-methylbenzenesulfonamide
Reaktionsgleichung
[CH:1]([C:4]1[N:5]=[C:6]([NH2:9])[S:7][CH:8]=1)([CH3:3])[CH3:2].[Cl:10][C:11]1[C:12]([CH3:21])=[C:13]([S:17](Cl)(=[O:19])=[O:18])[CH:14]=[CH:15][CH:16]=1>>[Cl:10][C:11]1[C:12]([CH3:21])=[C:13]([S:17]([NH:9][C:6]2[S:7][CH:8]=[C:4]([CH:1]([CH3:3])[CH3:2])[N:5]=2)(=[O:19])=[O:18])[CH:14]=[CH:15][CH:16]=1Komponenten
3
Versuchsvorschrift
The title compound was prepared from 4-isopropyl-1,3-thiazol-2-ylamine (METHOD I) and 3-chloro-2-methylbenzenesulfonyl chloride according to METHOD A, white foam, 80 mg (48% yield): HRMS Calcd (found) for C13H15ClN2O2S2 m/z 330.0263 (330.0257).
Quellen und Nachweise
- ORD-Eintrag
- ord-a282b427c4a54840918a7a9a05643bf6
- Quelldatensatz
- uspto-grants-2006_10
- Patentnummer
- US07125900B2
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