3-Bromo-5-((S)-1-methyl-pyrrolidin-2-ylmethoxy)-pyridine → HCID 67586395, compound

Participants

Reaction Conditions

Reaction Steps

To a 1.08 g (4 mmol) sample of 5-bromo-3-((1-methyl-2-(S)-pyrrolidinyl)methoxy)pyridine, prepared as in Example 56a above, dissolved in 40 mL of dry ether and cooled to 0° C. was added 6.0 mL of n-butylmagnesium chloride and 13.0 mg of Ni(dppp)Cl, and the reaction mixture was stirred for 5 hours at room temperature. The reaction was quenched by addition of satd NH4Cl, and the mixture was extracted with chloroform. The solvent was dried over MgSO4 and removed under vacuum, and the residue was purified of a column of silica gel, eluting with 100:1.25:0.025 chloroform:methanol:ammonium hydroxide. The product was converted into the title compound by treatment with HCl in ether according to Example 14c. MS (DCI/NH3) m/e: 259 (M+H)+. 1H NMR (D2O, 300 MHz) δ: 8.28 (d, J=3.0 Hz, 1H), 8.24 (s, 1H), 7.80 (m, 1H), 4.58 (dd, J=11.0, 3.0 Hz, 1H), 4.42 (dd, J=11.4, 5.5 Hz, 1H), 3.96 (m, 1H), 3.77 (m, 1H), 3.32-3.23 (m, 1H), 3.05 (s, 3H), 2.78 (t, J=7.3, 2H), 2.43-2.38 (m, 1H), 2.26-2.06 (m, 3H), 1.70-1.60 (m, 2H), 1.40-1.27 (m, 2H), 0.91 (t, J=7.4 Hz, 3H). Anal. Calc. for C15H24N2O.2 HCl.0.2 ether C, 56.46; H, 8.40; N, 8.33; Found C, 56.85; H, 8.73; N, 7.99. [α]25D =-7.30° (methanol).

Provenance & Evidence