Boron tribromide → 3-(1H-Pyrazol-4-yl)-1H-pyrrolo[2,3-b]pyridin-5-ol
反応式
C[O:2][C:3]1[CH:4]=[C:5]2[C:11]([C:12]3[CH:13]=[N:14][NH:15][CH:16]=3)=[CH:10][NH:9][C:6]2=[N:7][CH:8]=1.B(Br)(Br)Br>C(Cl)Cl>[NH:14]1[CH:13]=[C:12]([C:11]2[C:5]3[C:6](=[N:7][CH:8]=[C:3]([OH:2])[CH:4]=3)[NH:9][CH:10]=2)[CH:16]=[N:15]1参加物
4
反応条件
- 温度
- 0 °C
実験手順
To a suspension of 35 (25 mg, 0.12 mmol) in CH2Cl2 (2.0 mL), cooled to 0° C., was added a 1M solution of BBr3 (467 μL, 0.48 mmol) in CH2Cl2 and the reaction mixture stirred for 2 h at room temperature. More CH2Cl2 (2.0 mL) and BBr3 (467 μL) was added at r.t. and the stirring continued for 65 h. The reaction mixture was partitioned between AcOEt and saturated aqueous NaHCO3 and the layers separated. The aqueous phase was extracted with more AcOEt (4×), the combined organic extracts dried (MgSO4) and concentrated. The residue was purified by preparative LCMS (column LUNA 10 μ C18(2) 00G-4253-V0 250×50 mm) using water—MeCN (0.1% AcOH) as eluent (in gradient; flow 80 mL/min) to give 36 as a white solid (9.1 mg, 39%); 1H NMR (400 MHz, DMSO-d6) δ 7.49 (d, J=2.5 Hz, 1H), 7.57 (d, J=2.5 Hz, 1H), 7.86 (d, J=2.5 Hz, 1H), 7.90 (s, 2H), 9.05-9.20 (bs, 1H), 11.32 (bs, NH).