反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- 96 °C
PROCEDURE
实验过程
In 100 mL autoclave vessel, a solution of 3-(4-bromo-phenyl)-3-fluoro-azetidine-1-carboxylic acid tert-butyl ester (Intermediate from Step 5a; 5 g, 15.142 mmol, 1 eq) in ethanol (17.5 mL) was degassed with nitrogen gas for 30 minutes at room temperature. TEA (3.79 mL, 27.256 mmol, 1.8 eq), butyl vinyl ether (BVE, 3.91 mL, 30.282 mmol, 2 eq), 1,3-bis(diphenylphosphino)propane (DPPP, 0.375 g, 0.909 mmol, 0.06 eq) were added followed by addition of Pd(OAc)2 (0.102 g, 0.454 mmol, 0.03 eq.) at room temperature. Resulting reaction mixture was heated at 96° C. for 16 hours in an autoclave. After complete consumption of starting material, the reaction mixture was quenched with 1N HCl (5 mL, pH˜2-3) and stirred for 2 hours at room temperature. After 2 hours, the pH of reaction mixture was adjusted to 7 by addition of saturated NaHCO3 solution and extracted with ethyl acetate (3×50 mL). The combined organic layer was washed with brine (250 mL), dried over sodium sulphate and concentrated under reduced pressure to get crude compound as dark brown sticky oil (6.1 g, Crude). Crude compound was purified by column chromatography on silica gel using 230-400 silica mesh. Desired compound was eluted in 10% ethyl acetate in n-hexane to give product as off white semisolid (2.56 g, 57.66%). 1H NMR (400 MHz, CDCl3) δ: 1.46 (s, 9H), 2.61 (s, 3H), 4.20 (dd, J1=0.88 Hz, J2=10.28 Hz, 1H), 4.24 (dd, J1=0.92 Hz, J2=10.36 Hz, 1H), 4.39 (dd, J1=1.28 Hz, J2=10.24 Hz, 1H), 4.44 (dd, J1=1.28 Hz, J2=10.20 Hz, 1H), 7.55 (dd, J1=1.48 Hz, J2=8.48 Hz, 2H), 8.00 (d, J=7.96 Hz, 2H), LC-MS (m/z): 294.1 (M+H).
WORKUP
后处理
- customResulting
- customreaction mixture
- customAfter complete consumption of starting material
- customthe reaction mixture was quenched with 1N HCl (5 mL, pH˜2-3)
- waitAfter 2 hours
- customthe pH of reaction mixture
- extractionextracted with ethyl acetate (3×50 mL)
- washThe combined organic layer was washed with brine (250 mL)
- dry with materialdried over sodium sulphate
- concentrationconcentrated under reduced pressure
- customto get crude compound as dark brown sticky oil (6.1 g, Crude)
- customCrude compound was purified by column chromatography on silica gel using 230-400 silica mesh
- washDesired compound was eluted in 10% ethyl acetate in n-hexane