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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 70928Erstellt: 23. Oktober 2026

4-(Trifluoromethyl)benzenecarbothioyl chloride → N-[1-Cyano-2-(4,6-dichloro-2H-benzotriazol-2-yl)-1-methylethyl]-4-trifluoromethylthiobenzamide

https://huagongshe.com/de/reaction/70928

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-(Trifluoromethyl)benzenecarbothioyl chlorideHCID 19862484—
Edukt2-Amino-3-(4,6-dichloro-2H-benzotriazol-2-yl)-2-methylpropionitrileHCID 66619910—
ProduktN-[1-Cyano-2-(4,6-dichloro-2H-benzotriazol-2-yl)-1-methylethyl]-4-trifluoromethylthiobenzamideHCID 25122295—

Reaktionsschritte

Using a procedure similar to that described in Example 1, except using 2-amino-3-(4,6-dichloro-2H-benzotriazol-2-yl)-2-methylpropionitrile, described in Example 15, and 4-trifluoromethylthiobenzoyl chloride, the title compound was isolated as a white solid (50 mg, 20%). Rf=0.7 (1:1 EA/heptane). MS (ES): M/Z [M+H]=475. NMR: (400 MHz, DMSO-d6): 1.75 (s, 3H), 5.40-5.56 (m, 2H), 7.65 (m, 1H), 7.79-7.95 (m, 4H), 8.10 (m, 1H) and 8.95 (s, 1H). 19F NMR (376 MHz, DMSO-d6): −42.05 (s, 3F).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08822689B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-fbbe8b3d975c43da93f28066f74a5ee7
Quellennotizuspto-grants-2014_09