Reaktion #165672

Reaktionsgleichung

mixture

3-allyl-5-methylthiazol-2(3H)-imine hydrobromide

5-chloro-2-methoxybenzoylchloride

→

title compound

(Z)—N-(3-allyl-5-methylthiazol-2(3H)-ylidene)-5-chloro-2-methoxybenzamide

Reaktionsbedingungen

Vorschrift

A mixture of Example 232A (0.5 g) and 5-chloro-2-methoxybenzoylchloride (0.57 g) were processed according to the method of Example 227B to afford the title compound. 1H NMR (300 MHz, dimethylsulfoxide-d6) δ ppm 2.28 (d, J=1.4 Hz, 3H), 3.78 (s, 3H), 4.77 (d, 2H), 5.13 (dq, J=16.9, 1.3 Hz, 1H), 5.24 (dq, J=10.5, 1.4 Hz, 2H), 5.94-6.07 (m, 1H), 7.11 (d, 1H), 7.23 (q, J=1.4 Hz, 1H), 7.43 (dd, 1H), 7.68 (d, 1H); MS (ESI+) m/z 323 (M+H)+.

Quelle