反应详情

4-(4-bromo-2-cyclopropyl-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazol-5-yl)-2-chloropyrimidine (1 g, 2.4 mmol) was combined with aqueous 28% NH4OH solution (8 mL) in 1,4-dioxane (8 mL) and the resulting mixture was split evenly between two reaction vials. Each was irradiated in a microwave reactor for 40 minutes at 130° C. TLC analysis indicated complete reaction. The combined reactions were then diluted with water (100 mL) followed by extraction with EtOAc (100 mL). The EtOAc layer was washed with brine then dried (Na2SO4), and concentrated. Purification of the resulting residue by flash chromatography on silica gel using an EtOAc-hexanes gradient (0 to 60%) provided 0.87 g of (2.1 mmol, 91%) of 4-(4-bromo-2-cyclopropyl-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazol-5-yl)pyrimidin-2-amine as a white solid: LCMS (m/z): 410.0 (MH+), tR=0.81 minute.

1. customthe resulting mixture was split evenly between two reaction vials
2. customEach was irradiated in a microwave reactor for 40 minutes at 130° C
3. customreaction
4. extractionfollowed by extraction with EtOAc (100 mL)
5. washThe EtOAc layer was washed with brine
6. dry with materialthen dried (Na2SO4)
7. concentrationconcentrated
8. customPurification of the resulting residue by flash chromatography on silica gel using an EtOAc-hexanes gradient (0 to 60%)