“…1 H-NMR (400 MHz, CDCl 3 ): δ 2.44 (3H, s), 3.90 (3H, s), 6.60 (1H, dd, J = 0.9 Hz, J = 2.0 Hz), 7.14 (1H, dd, J = 2.0 Hz, J = 8.0 Hz), 7.15 (1H, d, J = 2 Hz), 7.24 (1H, s), 7.26 (1H, s), 7.46 (1H, d, J = 8.0 Hz), 7.65 (1H, d, J = 2.0 Hz). 13 5-(5-(2,6-bis(methylsulfanyl)pyridin-4-yl)-1H-tetrazol-1-yl)-1-methyl-1H-indole (11). Compound 11 was synthesized following the same methodology as compound 10, i.e., by using a solution consisting of compound 10 (560 mg, 1.6 mmol) in dry DMF (30 mL), sodium methanethiolate (224 mg, 3.20 mmol), and KOH (45 mg, 0.8 mmol).…”