HRID914000

反应详情

EQUATION

反应方程式

HRID 914000 的结构方程式

PROCEDURE

实验过程

tert-Butyl 4-phenyl-4-(((1-((2-(trimethylsilyl)ethoxy)methyl)-1H-indazol-7-yl)methoxy)methyl)piperidine-1-carboxylate (34 mg, 0.06 mmol) was treated with a trifluoroacetic acid/methylene chloride mixture (1:1, 2 mL) for 4 h. The solvent was removed in vacuo and the resulting crude mixture passed through a strong cation exchange column. After washing the column with several volumes of methanol, the product was eluted by washing the column with 2 M ammonia in methanol. The solvent was evaporated and the compound purified by reverse phase HPLC to afford 11 mg (56%) as a clear oil. 1H-NMR (CDCl3, 500 MHz) δ 8.91 (s, 1H), 8.24 (m, 1H), 7.76 (d, J=8.2 Hz, 1H), 7.40-7.43 (m, 2H), 7.28-7.35 (m, 4H), 7.22-7.25 (m, 1H), 4.81 (s, 2H), 3.48 (s, 2H), 3.38-3.41 (m, 2H), 2.96-2.97 (m, 2H), 2.39-2.41 (m, 4H). Mass spec.: 322.08 (MNa)+. Accurate mass spec.: m/z 322.1909 [MH]+, Δ=3.2 ppm.

WORKUP

后处理

  1. customThe solvent was removed in vacuo
  2. washAfter washing the column with several volumes of methanol
  3. washthe product was eluted
  4. washby washing the column with 2 M ammonia in methanol
  5. customThe solvent was evaporated
  6. customthe compound purified by reverse phase HPLC
  7. customto afford 11 mg (56%) as a clear oil