Identification | Back Directory | [Name]
5-Iodo-1H-indazole | [CAS]
55919-82-9 | [Synonyms]
5-IODOINDAZOLE 5-IODO (1H)INDAZOLE 1H-Indazole, 5-iodo- | [Molecular Formula]
C7H5IN2 | [MDL Number]
MFCD07781642 | [MOL File]
55919-82-9.mol | [Molecular Weight]
244.03 |
Chemical Properties | Back Directory | [Melting point ]
156 °C | [Boiling point ]
358.2±15.0 °C(Predicted) | [density ]
2.082±0.06 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Sealed in dry,2-8°C | [form ]
Crystalline Powder | [pka]
12.87±0.40(Predicted) | [color ]
Yellow to brown to purple | [InChI]
InChI=1S/C7H5IN2/c8-6-1-2-7-5(3-6)4-9-10-7/h1-4H,(H,9,10) | [InChIKey]
CGCHCLICSHIAAM-UHFFFAOYSA-N | [SMILES]
N1C2=C(C=C(I)C=C2)C=N1 |
Hazard Information | Back Directory | [Chemical Properties]
Solid | [Uses]
Used as a reactant for the preparation of indazole-pyridine based protein kinase B/Akt inhibitors. | [Synthesis]
General procedure for the synthesis of 5-iodo-1H-indazole from 5-aminoindazole:
1. a solution of sodium nitrite (2.7 g, 39.1 mmol) in water (40 ml) was slowly added dropwise to a solution of 1-H-indazol-5-amine (5.2 g, 39.1 mmol) in 6 at 0 °C.
2. N hydrochloric acid (73.7 ml) was added to the above mixture at 0°C.
3. the resulting mixture was added slowly and dropwise to a solution of potassium iodide (26.9 g, 162 mmol) in water (60 ml) at 0 °C.
4. The reaction mixture was stirred at room temperature for 3 hours.
5. After completion of the reaction, the reaction mixture was extracted with ethyl acetate (4 x 30 ml).
6. The organic phases were combined and washed sequentially with 10% w/v sodium thiosulfate solution (4 x 30 ml) and brine (2 x 30 ml).
7. The organic phase was dried with anhydrous magnesium sulfate and then concentrated to give a brown solid product.
8. Yield: 8.64 g (90% of theoretical). 9.
9. The structure of the product was confirmed by 3C-NMR (101 MHz, CDCl3, δppm): 84.4, 111.7, 125.6, 129.9, 133.4, 135.4, 139.0. | [References]
[1] Patent: WO2008/71451, 2008, A1. Location in patent: Page/Page column 47 [2] Patent: WO2014/170020, 2014, A1. Location in patent: Page/Page column 50 [3] Patent: US2009/156590, 2009, A1. Location in patent: Page/Page column 67; 69; 70 [4] Patent: US2012/28984, 2012, A1. Location in patent: Page/Page column 3 [5] Patent: WO2014/202580, 2014, A1. Location in patent: Page/Page column 164 |
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