Triethylamine → HCID 67311321, compound

Participants

Reaction Steps

To the mixture of 2-(5-amino-2-(N-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)sulfamoyl)phenyl)acetic acid (500 mg, 1.4 mmol) and azetidine hydrochloride (470 mg, 5 mmol) in DMF (5 ml), added PyBOP (730 mg, 1.4 mmol) then triethyl amine (1.1 ml, 8 mmol). Stirring was kept for 3 hours. Diluted with EtOAc, washed with 1N HCl, water and brine. Dried over anhydrous sodium sulfate. Concentrated, the residue was dissolved in DMSO and purified by prep HPLC (SunFire Prep C18 OBD 5 uM 30×50 mm column). The compound was obtained as white powder. MS calcd for (C18H20BN3O5S): 401.12. MS found (ESI negative): (M−H)−=400.1. 1H NMR (400 MHz, DMSO-d6) δ (ppm): 9.69 (s, 1H), 7.36 (d, J=1.6 Hz, 1H), 7.34 (d, J=8.8 Hz, 1H), 7.16 (d, J=8 Hz, 1H), 7.04 (dd, J=8.4 Hz, 1H), 6.34 (d, J=2.4 Hz, 1H), 6.30 (dd, J=8.8 Hz, 1H), 4.81 (s, 2H), 4.01 (t, J=7.2 Hz, 1H), 3.81 (t, J=7.6 Hz, 1H), 3.57 (s, 2H), 2.11 (m, 2H).

Provenance & Evidence