反应详情

To a stirred mixture of 9H-purin-6-ylamine (130 mg, 0.976 mmol) in DMF (5 mL) under an argon atmosphere was added NaH (60% in mineral oil, 40 mg, 0.976 mmol). After stirring for 10 min at RT, 2-bromomethyl-3-phenyl-1-(toluene-4-sulfonyl)-1H-indole (430 mg, 0.976 mmol) in DMF (10 mL) was added and stirring was continued for 15 min. The crude reaction mixture was loaded onto an Isolute® SCX-2 cartridge which was washed with MeOH and the product eluted with 2M NH3/MeOH. The product containing fractions were combined and concentrated under reduced pressure. The resulting residue was purified by column chromatography (Si—PCC, gradient 0-10% MeOH in DCM) affording 9-((3-phenyl-1-tosyl-1H-indol-2-yl)methyl)-9H-purin-6-amine as a white solid (370 mg, 77%). LCMS: RT 3.16 min [M+H]+ 495.1

1. stirringstirring
2. waitwas continued for 15 min
3. customThe crude reaction mixture
4. washwas washed with MeOH
5. washthe product eluted with 2M NH3/MeOH
6. additionThe product containing fractions
7. concentrationconcentrated under reduced pressure
8. customThe resulting residue was purified by column chromatography (Si—PCC, gradient 0-10% MeOH in DCM)