Reaktionsgleichung
Cl.[NH2:2][C:3]1[CH:7]=[C:6]([Cl:8])[S:5][C:4]=1[S:9]([NH2:12])(=[O:11])=[O:10].[CH2:13]([N:17]=[C:18]=S)[CH:14]([CH3:16])[CH3:15]>>[Cl:8][C:6]1[S:5][C:4]2[S:9](=[O:10])(=[O:11])[N:12]=[C:18]([NH:17][CH2:13][CH:14]([CH3:16])[CH3:15])[NH:2][C:3]=2[CH:7]=1Komponenten
3
Versuchsvorschrift
The title compound was prepared from 3-amino-5-chlorothiophene-2-sulfonamide hydrochloride and isobutyl isothiocyanate by a procedure analogous to the procedure described in example 3Bc-d; mp 262°-264° C.; 1H-NMR (DMSO-d6): δ 0.90 (d, 6H), 2.85 (m, 1H), 3.02 (t, 2H), 7.08 (s, 1H), 7.3 (br. s, 1H), 10.9 (br. s, 1H).
Quellen und Nachweise
- ORD-Eintrag
- ord-e13db33d3c07469c8ffc825053dae1aa
- Quelldatensatz
- uspto-grants-1999_03
- Patentnummer
- US05889002
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