反应详情

To a solution of 4-(3-(1H-indol-5-yl)-1-tosyl-1H-pyrrolo[2,3-b]pyridin-5-yl)benzaldehyde [Intermediate AJ] (0.11 g, 0.214 mmol) in CH2Cl2 (3 mL) was added 1-methylpiperazine (40 μL, 0.40 mmol) and sodium triacetoxyborohydride (68 mg, 0.32 mmol). The reaction mixture was stirred for 1 hr at room temperature, after which it was partitioned between CH2Cl2 and 1 M NaOH. The organic layer was separated, dried over MgSO4, and concentrated in vacuo. The residue was dissolved in 3:2 MeOH:acetone (5 mL), and 2 M NaOH (1.5 mL) was added. The resulting mixture was stirred at 65° C. for 30 min, after which it was partitioned between EtOAc and 1 M NaOH. The organic layer was separated, dried over MgSO4, filtered, and stripped to provide a residue that was subjected to preparatory HPLC to yield the title compound. HPLC retention time: 1.63 minutes; MS ESI (m/z) 422.4 (M+1)+, calc. 421.

1. customafter which it was partitioned between CH2Cl2 and 1 M NaOH
2. customThe organic layer was separated
3. dry with materialdried over MgSO4
4. concentrationconcentrated in vacuo
5. dissolutionThe residue was dissolved in 3:2 MeOH
6. additionacetone (5 mL), and 2 M NaOH (1.5 mL) was added
7. stirringThe resulting mixture was stirred at 65° C. for 30 min
8. customafter which it was partitioned between EtOAc and 1 M NaOH
9. customThe organic layer was separated
10. dry with materialdried over MgSO4
11. filtrationfiltered
12. customto provide a residue that