反应详情

4-{2-[(1,1-Dimethyl-2-oxoethyl)amino]-1,3-thiazol-4-yl}benzonitrile (290 mg, 1.07 mmol), prepared in step 1 of Example 83, was dissolved in methanol (8 mL) and tetrahydrofuran (2 mL) and then 1 g of molecular sieves was added. Acetic acid (0.12 mL, 2.1 mmol) and benzylamine (0.35 mL, 3.21 mmol) were added, followed by sodium cyanoborohydride (0.404 g, 6.42 mmol), and the mixture was stirred for 3 h. The mixture was diluted with ethyl acetate and washed with H2O, brine, dried over anhydrous MgSO4, filtered and concentrated to give 390 mg of crude product. This material was dissolved in 15 mL tetrahydrofuran and triethylamine (0.81 mL, 5.6 mmol) was added followed by triphosgene (0.48 g, 1.6 mmol). The mixture was stirred for 1 h, poured into saturated NaHCO3, diluted with methylene chloride and washed with H2O, 1N HCl, brine, dried over anhydrous MgSO4, filtered and concentrated. Flash chromatography (20% ethyl acetate/hexane) afforded the title compound (0.250 g, 60%) as a pale yellow solid. HRMS: calcd for C22H20N4OS+H+, 389.14306; found (ESI, [M+H]+), 389.1449; Analytical HPLC: 83.0% at 210-370 nm, 11.0 min; 84.4% at 252 nm, 11.0 min; the Xterra® RP18 column, 3.5%, 150×4.6 mm column, 1.2 mL/min, 85/15-5/95 (Ammon. Form. Buff. pH=3.5/ACN+MeOH) for 10 min, hold 4 min.

1. washwashed with H2O, brine
2. dry with materialdried over anhydrous MgSO4
3. filtrationfiltered
4. concentrationconcentrated
5. customto give 390 mg of crude product
6. stirringThe mixture was stirred for 1 h
7. washwashed with H2O, 1N HCl, brine
8. dry with materialdried over anhydrous MgSO4
9. filtrationfiltered
10. concentrationconcentrated