Pyrrolidine → HCID 11662298, compound

Participants

Reaction Steps

Compound is formed by reacting 2-chloro-N-[4-(2-morpholin-4-yl-ethoxy)-naphthalen-1-yl]-isonicotinamide and pyrrolidine under conditions described in general procedure A. 1H NMR (300 MHz, DMSO-d6) δ 10.38 (s, 1H), 8.21 (m, 2H), 7.83 (m, 1H), 7.59 (m, 2H), 7.42 (d, 1H), 7.10 (d, 1H), 7.02 (m, 2H), 4.31 (t, 2H), 3.61 (m, 4H), 3.49 (m, 4H), 2.87 (t, 2H), 2.58 (m, 4H), 1.99 (m, 4H). MS: 447.2 (M+1).

Provenance & Evidence