5-Fluoro-3-iodo-1H-indazole

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5-Fluoro-3-iodo-1H-indazole manufacturers

5-Fluoro-3-iodo-1H-indazole Basic information
Product Name:5-Fluoro-3-iodo-1H-indazole
Synonyms:5-FLUORO-3-IODO-1H-INDAZOLE 98%;5-Fluoro-3-iodo-1H-indazole;5-fluoro-3-iodo-1H-indazole(SALTDATA: FREE);1H-INDAZOLE,5-FLUORO-3-IODO-;5-fluoro-3-iodo-2H-indazole
CAS:858629-06-8
MF:C7H4FIN2
MW:262.02
EINECS:
Product Categories:
Mol File:858629-06-8.mol
5-Fluoro-3-iodo-1H-indazole Structure
5-Fluoro-3-iodo-1H-indazole Chemical Properties
Boiling point 361.4±22.0 °C(Predicted)
density 2.158±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka10.94±0.40(Predicted)
AppearanceOff-white to light yellow Solid
InChIInChI=1S/C7H4FIN2/c8-4-1-2-6-5(3-4)7(9)11-10-6/h1-3H,(H,10,11)
InChIKeyCZUPBTJBMHZBTJ-UHFFFAOYSA-N
SMILESN1C2=C(C=C(F)C=C2)C(I)=N1
Safety Information
HS Code 2933998090
MSDS Information
5-Fluoro-3-iodo-1H-indazole Usage And Synthesis
Synthesis
5-FLUORO-1H-INDAZOLE

348-26-5

5-Fluoro-3-iodo-1H-indazole

858629-06-8

5-Fluoro-1H-indazole (2.0 g, 14.0 mmol) was used as raw material and dissolved in DIVIF (50 mL). To this solution, iodine (7.46 g, 28.0 mmol) and potassium hydroxide (2.4 g, 42 mmol) were added sequentially at 0 °C. The reaction mixture was stirred at 0 °C for 0.5 h and then gradually warmed up to room temperature. The reaction process was monitored by thin layer chromatography (TLC). After completion of the reaction, the mixture was filtered and the filtrate was concentrated under reduced pressure to give the crude product. The crude product was purified by silica gel column chromatography (eluent: petroleum ether/ethyl acetate=3/1) to afford 5-fluoro-3-iodo-1H-indazole (3.7 g, yield: 96.1%) as a white solid. The structure of the product was confirmed by 1H NMR (400 MHz, DMSO-d6): δ=13.64 (s, 1H), 7.63 (dd, J=4.8,4.4 Hz, 1H), 7.38-7.30 (m, 1H), 7.20 (dd, J=6.4,2.4 Hz, 1H).

References[1] Patent: WO2018/132372, 2018, A1. Location in patent: Paragraph 01229
[2] Patent: WO2018/188590, 2018, A1. Location in patent: Paragraph 00437
[3] Synthesis, 2011, # 19, p. 3089 - 3098
[4] Journal of Medicinal Chemistry, 2014, vol. 57, # 12, p. 5419 - 5434
[5] Molecules, 2018, vol. 23, # 8,
5-Fluoro-3-iodo-1H-indazole Preparation Products And Raw materials
Raw materials5-Fluoro-1H-indazole-->N,N-Dimethylformamide-->Potassium hydroxide-->iodine
Preparation ProductsMethyl 5-fluoro-1H-indazole-3-carboxylate
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