HRID1972924

反应详情

EQUATION

反应方程式

HRID 1972924 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

To a solution of tert-butyl 3-[4-amino-5-(2-benzyl-2H-indazol-6-yl)pyrrolo[2,1-f][1,2,4]triazin-7-yl]-3-hydroxypiperidine-1-carboxylate (270 mg, 0.500 mmol) in MeOH (2.5 mL) was added 4M HCl in dioxane (1.25 mL). The mixture was stirred at rt for 17 h. The mixture was concentrated and the residue was dissolved in 3:1 CHCl3/isopropanol (25 mL). The mixture was washed with saturated, aqueous NaHCO3 (25 mL), brine, dried (Na2SO4) and concentrated to dryness to afford 211 mg (96%) of the desired product, which was approximately 50% pure. ES-MS m/z 440.19 [M+H]+, HPLC RT (min) 1.97. 50 mg of material was purified by preparative HPLC using a gradient elution from 15% to 40% acetonitrile in water followed by filtration through an acidic resin, washing with MeOH. The product was eluted with 2M NH3 in MeOH and the filtrate was concentrated to provide 28 mg of pure desired product. 1H NMR (400 MHz, DMSO-d6) δ 8.54 (s, 1 H), 7.89 (s, 1 H), 7.80 (d, 1 H), 7.58 (s, 1 H), 7.27-7.37 (m, 5 H), 7.13 (dd, 1.36 Hz, 1 H), 6.69 (s, 1 H), 5.64 (s, 2 H), 5.19 (s, 1 H), 2.77-2.93 (m, 2 H), 2.43-2.54 (m, 3 H), 2.12 (br s, 1 H), 1.68-1.88 (m, 2 H), 1.33-1.46 (m, 1 H); ES-MS m/z 439.92 [M+H]+, HPLC RT (min) 2.06.

WORKUP

后处理

  1. concentrationThe mixture was concentrated
  2. dissolutionthe residue was dissolved in 3:1 CHCl3/isopropanol (25 mL)
  3. washThe mixture was washed with saturated, aqueous NaHCO3 (25 mL), brine
  4. dry with materialdried (Na2SO4)
  5. concentrationconcentrated to dryness