反应详情

Tetrabutylammonium fluoride (1.0M in THF, 1.5 mL) is added to a suspension of PS-isocyanate resin (0.4 g) in THF (1.5 mL) and the mixture is stirred at RT for 2 h. The resin is filtered off and the filtrate is added to a solution of 2-((E)-4-{3-benzyloxy-4-[1,1,4-trioxo-5-(2-trimethylsilanylethyl)-1,2,5-thiadiazolidin-2-yl]-phenyl}-but-3-enyl)-isoindole-1,3-dione (90 mg, 0.146 mmol) in THF (1 mL). The reaction is stirred at 65° C. for 1 h and at RT for 18 h. The mixture is cooled and concentrated. The residue is partitioned between EtOAc and water and the organic layer is washed with 2N HCl (3×) and saturated aqueous sodium chloride. The organic layer is dried over Na2SO4 and the solvent removed under reduced pressure to give the title compound: (M−1)−=516.

1. filtrationThe resin is filtered off
2. stirringThe reaction is stirred at 65° C. for 1 h and at RT for 18 h
3. temperatureThe mixture is cooled
4. concentrationconcentrated
5. customThe residue is partitioned between EtOAc and water
6. washthe organic layer is washed with 2N HCl (3×) and saturated aqueous sodium chloride
7. dry with materialThe organic layer is dried over Na2SO4
8. customthe solvent removed under reduced pressure