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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1716233Erstellt: 25. Oktober 2026

2-Chloro-1-(1,2,3,4-tetrahydroquinolin-1-yl)ethan-1-one → 1-(3,4-Dihydro-2H-quinolin-1-yl)-2-(5-trifluoromethyl-benzothiazol-2-ylsulfanyl)-ethanone

https://huagongshe.com/reaction/1716233

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Chloro-1-(1,2,3,4-tetrahydroquinolin-1-yl)ethan-1-oneHCID 240137—
Edukt5-(trifluoromethyl)-1,3-benzothiazole-2-thiolHCID 178419087—
Produkt1-(3,4-Dihydro-2H-quinolin-1-yl)-2-(5-trifluoromethyl-benzothiazol-2-ylsulfanyl)-ethanoneHCID 5946789780%

Reaktionsschritte

The title compound was synthesized according to General Procedure A using compound 4 as the electrophile and 5-(trifluoromethyl)benzo[d]thiazole-2-thiol as the nucleophile to yield 23 as a white solid (80%): MS m/z: 409 (M+H)+. Anal. Calcd. For, C19H15F3N2OS2: C, 55.87; H, 3.70; N, 6.86; S, 15.70; F, 13.95. Found: C, 55.79; H, 3.71; N, 6.92; S, 15.67; F, 14.07.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07803790B2
Quelldatensatzuspto-grants-2010_09
ORD IDord-c29d1931169d44d697a41d6e63722a6e
Quellennotizuspto-grants-2010_09