HRID2170170

反应详情

EQUATION

反应方程式

HRID 2170170 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
100 °C

PROCEDURE

实验过程

To a stirred solution of N-benzyl-2-chloro-5-phenylpyrrolo[2,1-f][1,2,4]triazin-4-amine (0.500 g, 1.49 mmol) dissolved in DMF (5 mL) was added sodium cyanide (0.366 g, 7.47 mmol). The reaction mixture was heated to 100° C. for 24 h and cooled. Reaction was quenched by adding ice cold water (100 mL) and was extracted with EtOAc (50×3 mL). The organic layer was separated and dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by column chromatography using CombiFlash (REDISEP®, silica gel, 24 g, 10% EtOAc/hexanes) to afford 4-(benzylamino)-5-phenylpyrrolo[2,1-f][1,2,4]triazine-2-carbonitrile (0.200 g, 41.2%). LCMS Condition B-45: retention time 2.95 min, [M−1]=324.2. HPLC Condition B-2: retention time 25.49 min, Purity 98.76%. 1H NMR (400 MHz, DMSO-d6) δ ppm 4.68 (s, 2H), 6.92-6.96 (m, 2H), 7.26 (m, 10H), 7.86 (d, J=2.8 Hz, 1H).

WORKUP

后处理

  1. temperaturecooled
  2. customReaction
  3. customwas quenched
  4. additionby adding ice cold water (100 mL)
  5. extractionwas extracted with EtOAc (50×3 mL)
  6. customThe organic layer was separated
  7. dry with materialdried over anhydrous sodium sulfate
  8. concentrationconcentrated under reduced pressure
  9. customThe residue was purified by column chromatography