反应详情

To a solution of (R)-tert-butyl(1-(2-(1-(cyclopropylmethyl)-1H-pyrrolo[2,3-b]pyridin-2-yl)-1-methyl-1H-benzo[d]imidazole-5-carbonyl)piperidin-3-yl)carbamate (3.402 g, 6.44 mmol) in dichloromethane (DCM) (40 ml) was added TFA (9 ml, 118 mmol) dropwise. The reaction mixture was stirred for 3 hours. The reaction mixture was concentrated under vacuum to afford a yellow oil. The oil was dissolved in methanol and loaded onto a 70 g SCX cartridge. The column was washed with MeOH (2CV) and the product collected as the free base with 2M ammonia in methanol (3CV). The product was concentrated in vacuo and dried under vacuum to afford a yellow solid. This was dissolved in hot ethanol and concentrated in vacuo. It was again dissolved in hot ethanol, concentrated in vacuo and dried under vacuum to yield the title compound as a yellow solid (2.61 g).

1. concentrationThe reaction mixture was concentrated under vacuum
2. customto afford a yellow oil
3. washThe column was washed with MeOH (2CV)
4. customthe product collected as the free base with 2M ammonia in methanol (3CV)
5. concentrationThe product was concentrated in vacuo
6. customdried under vacuum
7. customto afford a yellow solid
8. concentrationconcentrated in vacuo
9. dissolutionIt was again dissolved in hot ethanol
10. concentrationconcentrated in vacuo
11. customdried under vacuum