5-Bromopyridine-2-carboxylic acid → 2-(Azetidin-1-ylcarbonyl)-5-bromopyridine

Participants

Reaction Steps

The title compound was prepared in a similar manner as described for Intermediate 161a, from 5-bromopyridine-2-caboxylic acid (1.50 g, 7.43 mmol) and azetidine hydrochloride (954 mg, 10.2 mmol) to give a yellow solid (1.38 g, 77% yield). 1H NMR (400 MHz, CDCl3) δ 8.58 (d, J=2.02 Hz, 1 H) 7.93-7.99 (m, 1 H) 7.90 (d, J=2.27 Hz, 1 H) 4.65 (t, J=7.71 Hz, 2 H) 4.20 (dd, J=8.34, 7.33 Hz, 2 H) 2.27-2.36 (m, 2 H); LCMS for C9H9BrN2O m/z 241.00 (M+H)+.

Provenance & Evidence