4,6-DIFLUORO-3-IODOINDAZOLE
4,6-DIFLUORO-3-IODOINDAZOLE Basic information
- Product Name:
- 4,6-DIFLUORO-3-IODOINDAZOLE
- Synonyms:
-
- 4,6-Difluoro-3-iodo-1H-indazole
- 4,6-DIFLUORO-3-IODOINDAZOLE
- 3-Iodo-4,6-difluoro indazole
- 4,6-Difluoro-3-iodo-2H-indazole
- 1H-Indazole, 4,6-difluoro-3-iodo-
- CAS:
- 887567-79-5
- MF:
- C7H3F2IN2
- MW:
- 280.01
- Mol File:
- Mol File
4,6-DIFLUORO-3-IODOINDAZOLE Chemical Properties
- Boiling point:
- 355.7±37.0 °C(Predicted)
- Density
- 2.229±0.06 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2–8 °C
- pka
- 10.47±0.40(Predicted)
4,6-DIFLUORO-3-IODOINDAZOLE Usage And Synthesis
Synthesis
885520-26-3
887567-79-5
Example 10: Synthesis of 1.2-(4,6-difluoro-1-methyl-1H-indazol-3-yl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxyisopropylamide Step 1: Synthesis of 4,6-difluoro-3-iodo-1H-indazole At room temperature, 4,6-difluoro-1H-indazole (1.16 g, 7.53 mmol) was dissolved in DMF (60 mL) and potassium hydroxide (1.27 g, 22.6 mmol) and iodine (2.87 g, 11.3 mmol) were added sequentially. The reaction mixture was stirred at room temperature for 2 h. The reaction solution was maroon in color. After completion of the reaction, the reaction was quenched with 10% Na2S2O3 aqueous solution and diluted with water. The mixture was extracted with EtOAc (2×). The organic phases were combined, washed sequentially with water, saturated LiCl solution and saturated NaCl solution, dried over MgSO4 and concentrated to give 4,6-difluoro-3-iodo-1H-indazole (2.18 g) as a light brown solid.
References
[1] Patent: WO2013/30138, 2013, A1. Location in patent: Page/Page column 262; 263
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