4-Pentylbenzoyl chloride → Methyl 3-methyl-2-(N-methyl-5-(4-(4-pentylbenzamido)phenyl)thiazole-2-carboxamido)butanoate

Participants

Reaction Steps

The title compound was synthesized analogous to Example 27, using 4-pentylbenzoyl chloride and intermediate 4. Yield: 59%; 1H NMR (DMSO-d6, 300 MHz): δ 10.38 (s, 1H), 8.86 (d, 1H), 7.95 (m, 4H), 7.78 (d, 2H), 7.37 (d, 2H), 6.27-4.76 (d, 1H), 3.68 (s, 3H), 3.47-2.95 (s, 3H), 2.68 (t, 2H), 2.38 (m, 1H), 1.63 (m, 2H), 1.30 (m, 4H), 1.03 (m, 3H), 0.90 (dd, 6H); MS (ESI) m/z 522.2 [M+H]+.

Provenance & Evidence