反应详情

A nitrogen purged 500 mL three-neck flask is charged with 4-fluoro-α-(2-methyl-1-oxopropyl)-γ-oxo-N,β-diphenylbenzenebutanamide (Baumann, supra) (13.6 g, 0.032 mol), (4R-cis)-6-(2-aminoethyl)-2,2-dimethyl-N,N-diphenyl-1,3-dioxane-4-acetamide (10.0 g, 0. 027 mol), heptane (100 mL), pivalic acid (3 g), tetrahydrofuran (50 mL), and toluene (60 mL). The mixture is heated to reflux for 48 hours, cooled to room temperature, and diluted with toluene (300 mL). The solution is washed with 0.5N aqueous sodium hydroxide (150 mL), followed by 0.5N aqueous hydrochloric acid (250 mL), and concentrated by vacuum distillation to a foam. The product, (4R-cis)-1-[2-[6-[2-(diphenylamino)-2-oxoethyl]-2,2-dimethyl-1,3-dioxan-4-yl]ethyl]-5-(4-fluorophenyl)-2-(1-methyl ethyl)-N,4-diphenyl-1H-pyrrole-3 -carboxamide, is used in the next step without further purification. Fourier Transform Infrared Spectroscopy (FTIR) (KBr) 3450, 2860, 1650, 1620 cm-1 ;

1. customA nitrogen purged 500 mL three-neck flask
2. temperatureThe mixture is heated
3. temperatureto reflux for 48 hours
4. washThe solution is washed with 0.5N aqueous sodium hydroxide (150 mL)
5. concentrationconcentrated by vacuum distillation to a foam
6. customThe product, (4R-cis)-1-[2-[6-[2-(diphenylamino)-2-oxoethyl]-2,2-dimethyl-1,3-dioxan-4-yl]ethyl]-5-(4-fluorophenyl)-2-(1-methyl ethyl)-N,4-diphenyl-1H-pyrrole-3 -carboxamide, is used in the next step without further purification