Methoxyacetic Acid → N-{2-[(4-{[3-Chloro-4-(pyridin-2-ylmethoxy)phenyl]amino}quinazolin-5-yl)oxy]ethyl}-2-methoxyacetamide

Participants

Reaction Steps

The procedure described in Example 1 was repeated using methoxyacetic acid and 5-(2-aminoethoxy)-N-[3-chloro-4-(pyridin-2-ylmethoxy)phenyl]quinazolin-4-amine (obtained as described in Example 2.6, preparation of starting materials) to give the title compound in 50% yield; NMR spectrum (DMSO-d6) 3.20 (s, 3H), 3.68 (m, 2H), 3.73 (s, 2H), 4.38 (t, 2H), 5.29 (s, 2H), 7.14 (d, 1H), 7.21 (d, 1H), 7.34 (m, 2H), 7.55 (t, 1H), 7.71 (t, 1H), 7.86 (t, 1H), 7.97 (d, 1H), 8.17 (m, 1H), 8.44 (s, 1H), 8.58 (d, 1H), 9.81 (s, 1H); Mass Spectrum MH+ 494.

Provenance & Evidence