反应 #9676

ord-d6c3407adb094fd186601245d5ddcf08

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    浓缩was then concentrated in vacuo
  2. 2
    温度heated
  3. 3
    温度at reflux for 15 minutes
  4. 4
    过滤The hot suspension was filtered
  5. 5
    洗涤rinsing with hot ethanol
  6. 6
    浓缩the filtrate was concentrated in vacuo

实验过程

The procedure used was similar to that reported in J. Med. Chem. 40:811–818, 1997. A solution of 1,2-diamino-4,5-difluorobenzene (500 mg, 3.47 mmol) in water (5 mL) was cooled to 0° C. and then treated with a solution of cyanogen bromide (0.83 mL, 4.16 mmol, 5 M in acetonitrile) and solid sodium bicarbonate (583 mg, 6.94 mmol). The solution was stirred at rt overnight and was then concentrated in vacuo. The dark residue was suspended in ethanol and heated at reflux for 15 minutes. The hot suspension was filtered, rinsing with hot ethanol, and the filtrate was concentrated in vacuo to afford 5,6-difluoro-1H-benzimidazol-2-amine (580 mg, 59%), which was used in the next step without further purification. LC-MS m/z 170.2 (MH+), ret. time 0.85 min; 1H NMR (300 MHz, DMSO-d6) δ 6.30 (br s, 2H), 7.06 (dd, 2H), 10.79 (br s, 1H).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07091228B2uspto-grants-2006_08