5-chloro-2-(trifluoromethyl)-1,8-Naphthyridine → (5-Methyl-2-phenylsulfanyl-phenyl)-(7-trifluoromethyl-[1,8]naphthyridin-4-yl)-amine

関与物質

反応手順

The product from Example 7d (65 mg, 0.28 mmol) and the product from Example 1f (61.5 mg, 0.28 mmol) was reacted 28 h following the procedure from Example 1g giving the title compound as a hydrochloride salt after trituration with ether giving (131 mg, 99%). 1H NMR (300 MHz, DMSO-d6) δ ppm: 6.43 (d, J=6.99 Hz, 1H) 7.23 (m, 4H) 7.35 (m, 4H) 8.39 (d, J=8.82 Hz, 1H) 8.55 (d, J=6.99 Hz, 1H) 9.48 (d, J=8.46 Hz, 1H) 11.55 (brs, 1H); MS (ESI+) m/z 412 (M−Cl)+; (ESI−) m/z 410 (M−HCl)−.

情報源と証拠