2-Amino-5-methylpyridine → HCID 58869965, compound

Participants

Reaction Steps

The product from Example 1, Part C and 5-methylpyridin-2-ylamine were reacted as described in Example 5. After evaporation of the reaction solvent the residue was partitioned between water and EtOAc, and the organic phase was washed with EtOAc. The combined organics were washed with brine, dried (Na2SO4), filtered, and evaporated. The title compound was obtained by silica gel chromatography. 1H NMR (400 MHz, CDCl3) δ 8.43 (br s, 1H), 8.09 (m, 1H), 8.02 (d, J=9 Hz, 1H), 7.51 (m, 1H), 7.21 (d, J=9 Hz, 2H), 6.83 (d, J=9 Hz, 2H), 5.07 (d, J=15 Hz, 1H), 4.61 (s, 1H), 4.14 (d, J=15 Hz, 1H), 3.77 (s, 3H), 2.89 (m, 2H), 2.30 (s, 3H), 1.95 (s, 3H), 1.83 (s, 3H). MS: m/z (MH+) 412.

Provenance & Evidence