Tetrahydrofuran → 2-(6-(2-(2,4-difluorophenyl)-6,7-dihydro-5H-pyrrolo[1,2-a]imidazol-3-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)propan-2-ol

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Reaction Steps

A 100 mL round bottom flask was charged with 1-(6-(2-(2,4-difluorophenyl)-6,7-dihydro-5H-pyrrolo[1,2-a]imidazol-3-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)ethanone (2.74 g, 7.20 mmol, Example #35, Step G). THF (36.0 mL) was added and the mixture was stirred at ambient temperature for about 15 min. The slurry was cooled to about −40° C. and methylmagnesium chloride (3.0 M in THF, 6.00 mL, 18.0 mmol) was added slowly while keeping the internal temperature between about −40-−30° C. After about 15 min, the mixture was cooled to about −55° C. followed by the slow addition of a saturated solution of ammonium chloride (about 10 mL). The mixture was then warmed to ambient temperature and diluted with water (50 mL) and DCM (75 mL). The layers were separated. The aqueous layer was extracted with DCM (2×50 mL) then the combined organic extracts were dried over MgSO4, filtered, and concentrated under reduced pressure to give a foam. The material was dissolved in 95:5 DCM/MeOH (about 20 mL) with warming and sonication and then loaded onto a 120 g silica column and eluted with 94:6 DCM/MeOH (about 1 L) followed by 92:8 DCM/MeOH (about 500 mL). Concentration of the fractions containing product under reduced pressure gave the title compound as a foam (2.88 g, 91%) that contained about 9 wt % DCM by 1H NMR. This material was combined with a second batch of the title compound (3.4 g, also contained about 9 wt % DCM). The combined material (5.7 g) was dissolved into ACN (150 mL), followed by a rapid precipitation of the title compound as an off-white powder. The material was collected by filtration and dried in a vacuum oven at 70° C. to give the title compound (4.69 g, 82% recovery): LC/MS (Table 1, Method g) Rt=1.58 min; MS m/z: 397.2 (M+H)+.

Provenance & Evidence