(2,6-Dichloropyridin-3-yl)methanol → CID 59589311

反応式

[Cl:1][C:2]1[C:7]([CH2:8]O)=[CH:6][CH:5]=[C:4]([Cl:10])[N:3]=1.BrCC1C(Cl)=NC(Cl)=CC=1.[CH3:21][C:22]1[N:27]=[C:26]([SH:28])[N:25]=[C:24]([OH:29])[CH:23]=1>C(N(CC)CC)C>[Cl:1][C:2]1[C:7]([CH2:8][S:28][C:26]2[N:25]=[C:24]([OH:29])[CH:23]=[C:22]([CH3:21])[N:27]=2)=[CH:6][CH:5]=[C:4]([Cl:10])[N:3]=1

参加物

実験手順

The crude (2,6-dichloropyridin-3-yl)methanol was converted to 3-(bromomethyl)-2,6-dichloropyridine, which was then reacted with 6-methyl-2-sulfanylpyrimidin-4-ol in the presence of triethylamine to provide 2-{[(2,6-dichloropyridin-3-yl)methyl]sulfanyl}-6-methylpyrimidin-4-ol as a white solid (0.822 g, 82% yield); 1H NMR (400 MHz, DMSO-d6): δ 2.15 (s, 3H), 4.36 (s, 2H), 5.95 (bs, 1H), 7.40 (d, J=8.0 Hz, 1H), 8.01 (d, J=8.0 Hz, 1H); M+ 302.5.