HRID1621707

反应详情

EQUATION

反应方程式

HRID 1621707 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
80 °C

PROCEDURE

实验过程

A mixture of N,N-bis(4-methoxybenzyl)-4-(2-(2-methoxypyrimidin-5-ylamino)-5-((4-(methylsulfonyl)piperazin-1-yl)methyl)pyridin-3-yl)-6-methyl-1,3,5-triazin-2-amine (301 mg, 0.414 mmol) in trifluoroacetic acid (638 μL, 8.28 mmol) was treated with a couple of drops of trifluoromethanesulfonic acid and the mixture was heated at 80° C. overnight. After cooling, the mixture was concentrated and the residue was dissolved in 5% (2 M NH3 in MeOH)/DCM (5 mL) and the crude product was adsorbed onto a plug of silica gel and chromatographed through a Redi-Sep pre-packed silica gel column (pure DCM→3% MeOH in DCM). The isolated yellow solid was dissolved in DMSO and was subjected to a reversed phase preparative HPLC purification (10% MeCN in H2O to 100% MeCN w/0.10% (v/v) TFA). The product fraction was basified with saturated NaHCO3 (aq), extracted with dichloromethane (3×20 mL) and the combined organic layers were dried over Na2SO4, filtered, and concentrated to give 4-(2-(2-methoxypyrimidin-5-ylamino)-5-((4-(methylsulfonyl)piperazin-1-yl)methyl)pyridin-3-yl)-6-methyl-1,3,5-triazin-2-amine (65 mg, 0.134 mmol, 32.3% yield) as a bright yellow solid. 1H NMR (400 MHz, d6-DMSO) δ 11.78 (s, 1H); 9.03 (s, 2H); 8.73 (d, J=1.56 Hz, 1H); 8.23 (d, J=1.76 Hz, 1H); 7.91 (br. s., 1H); 7.75 (br. s., 1H); 3.91 (s, 3H); 3.50 (s, 2H); 3.11 (br. s., 4H); 2.86 (s, 3H); 2.46-2.49 (m, 4H); 2.44 (s, 3H). m/z (ESI, +ve ion) 486.8 (M+H)+.

WORKUP

后处理

  1. temperatureAfter cooling
  2. concentrationthe mixture was concentrated
  3. dissolutionthe residue was dissolved in 5% (2 M NH3 in MeOH)/DCM (5 mL)
  4. customchromatographed through a Redi-Sep pre-packed silica gel column (pure DCM→3% MeOH in DCM)
  5. dissolutionThe isolated yellow solid was dissolved in DMSO
  6. customwas subjected to a reversed phase preparative HPLC purification (10% MeCN in H2O to 100% MeCN w/0.10% (v/v) TFA)
  7. extractionextracted with dichloromethane (3×20 mL)
  8. dry with materialthe combined organic layers were dried over Na2SO4
  9. filtrationfiltered
  10. concentrationconcentrated