HRID1640983

反应详情

EQUATION

反应方程式

HRID 1640983 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

2-Amino-N-(5-benzenesulfonyl-1H-indazol-3-yl)-4-(4-methyl-piperazin-1-yl)-benzamide (245 mg, 0.5 mmol) was dissolved in dichloromethane (5 mL) and trifluoroacetic acid (0.77 mL, 10 mmol), treated first with tetrahydro-pyran-4-one (0.055 mL, 0.6 mmol) and then with tetramethylammonium triacetoxyborohydride (197 mg, 0.75 mmol). The reaction was stirred at room temperature overnight then additional ketone (0.055 mL, 0.6 mmol) and hydride (2 portions: 197 mg first and 50 mg after a couple of hours) were added. After additional stirring overnight the volatiles were removed under reduced pressure. Dichloromethane was added and the organic phase was washed with aqueous sodium hydrogen carbonate, dried over sodium sulfate and evaporated. The crude product was purified by flash chromatography over silica gel (eluent: dichloromethane/methanol/33% NH4OH in 95:5:1 ratio) affording 186 mg of product still containing some impurities. Further purification by preparative HPLC (basic method) gave 80 mg of title compound.

WORKUP

后处理

  1. stirringAfter additional stirring overnight the volatiles
  2. customwere removed under reduced pressure
  3. additionDichloromethane was added
  4. washthe organic phase was washed with aqueous sodium hydrogen carbonate
  5. dry with materialdried over sodium sulfate
  6. customevaporated
  7. customThe crude product was purified by flash chromatography over silica gel (eluent: dichloromethane/methanol/33% NH4OH in 95:5:1 ratio)