HRID246230

反应详情

EQUATION

反应方程式

HRID 246230 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To a 20 ml vial containing 2-(6-fluoro-1-methyl-1H-indazol-3-yl)-5-(2-trimethylsilanylethoxymethyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid ((R)-1-benzyl-pyrrolidin-3-yl)-amide (51 mg, 0.085 mmol) dissolved in THF (1 ml) was added TBAF (1.0 M in THF, 1.0 ml, 1.0 mmol). The vial was backfilled with nitrogen then sealed and placed in heat block at 80° C. for 3 h. The reaction was cooled to room temperature, quenched with acetone (2 ml) and sat'd NaHCO3 (20 ml). The mixture was stirred for 1 h then extracted with EtOAc and the organics washed with brine. The aqueous was again extracted with EtOAc and the organics washed with brine. The organics were combined, dried over MgSO4, filtered and concentrated. The crude was dissolved in MeOH and EtOAc, supported on Celite, and purified by flash chromatography (4 g silicycle) with 0% to 10% MeOH in dichloromethane to 10% MeOH in EtOAc. The appropriate fractions were combined and concentrated. The solid was triturated with dichloromethane, Et2O, and hexanes to isolate 11 mg (29%) of 2-(6-fluoro-1-methyl-1H-indazol-3-yl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid ((R)-1-benzyl-pyrrolidin-3-yl)-amide as a white solid. LC-MS (M+H)+=470; 1H NMR (300 MHz, DMSO-d6) δ: 12.87 (br. s., 1H), 9.10 (s, 1H), 8.34-8.54 (m, 3H), 7.68 (dd, J=9.8, 1.8 Hz, 1H), 7.11-7.26 (m, 5H), 6.97 (td, J=9.1, 1.9 Hz, 1H), 4.60 (br. s., 1H), 4.16 (s, 3H), 3.61 (s, 2H), 2.82-2.97 (m, 1H), 2.58-2.75 (m, 2H), 2.29-2.44 (m, 2H), 1.75 (br. s., 1H).

WORKUP

后处理

  1. customthen sealed
  2. customquenched with acetone (2 ml) and sat'd NaHCO3 (20 ml)
  3. extractionthen extracted with EtOAc
  4. washthe organics washed with brine
  5. extractionThe aqueous was again extracted with EtOAc
  6. washthe organics washed with brine
  7. dry with materialdried over MgSO4
  8. filtrationfiltered
  9. concentrationconcentrated
  10. dissolutionThe crude was dissolved in MeOH
  11. custompurified by flash chromatography (4 g silicycle) with 0% to 10% MeOH in dichloromethane to 10% MeOH in EtOAc
  12. concentrationconcentrated
  13. customThe solid was triturated with dichloromethane, Et2O, and hexanes