Structure of 22297-71-8
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The BI-3802 was designed by Boehringer Ingelheim and could be obtained free of charge through the Boehringer Ingelheim open innovation portal opnMe.com, associated with its negative control.
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CAS No. : | 22297-71-8 |
Formula : | C9H6INO |
M.W : | 271.06 |
SMILES Code : | IC1=CC=C2C(O)=CC=NC2=C1 |
MDL No. : | MFCD06659038 |
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
95% | With thionyl chloride; N,N-dimethyl-formamide; at 90℃; for 18.0h; | Thionyl chloride [130 ml] was added to Intermediate 4 (7.9 g, 29.15 mmol) to give a suspension. A few drops of dimethylformamide were added and the mixture was heated in an oil bath at 90° C. under nitrogen for approximately 18 hours. The solution was cooled and concentrated in vacuo. The resulting residue was azeotroped with toluene and the solid obtained was triturated using diethyl ether. A pale yellow solid was collected by filtration and washed with more ether to provide the desired product (9.003 g, 95percent). |
80% | With trichlorophosphate; for 2.0h;Heating / reflux; | Compound 6-F (4.5 g) was dissolved in 30 mL of POCI3. The solution was heated to reflux for 2 hours. The excess amount of POCI3 was removed by evaporation under vacuum. The residue was basified with NH40H and extracted with EtOAc. The organic layer was concentrated to give 3.95 g (80percent yield) of 4-chloro-7-iodoquinoline 6-G as a yellow solid. |
With trichlorophosphate; at 130℃; for 2.5h; | A mixtureof 3-iodoaniline (3, 5.75 g, 26 mmol)and diethyl ethoxymethylenemalonate (4,5.67 g, 26 mmol) was stirred at room temperature until homogeneous, then heatedat 100 °C for 3 hours under a continuous stream of argon to help removeethanol. After this time, diphenyl ether (25 g) was added to the moltenacrylate 5 and the mixture heated at250-260 °C for 3 hours (a precipitate formed). After cooling down to roomtemperature, petroleum ether (50 mL) was added and the precipitate collected byfiltration. The solid was washed with petroleum ether and allowed to dry toobtain 6. This intermediate ester 6 (3.40 g, 10 mmol) was refluxed in 10percent aqueous sodium hydroxide for 1.5 hours and, after cooling down to roomtemperature, the solution was acidified with concentrated hydrochloric acid.The precipitate was filtered, washed with water and dried. A suspension of theresulting solid in diphenyl ether (10 g) was then heated at 250-270 °C for 6hours until effervescence ceased. When cold, the mixture was diluted withpetroleum ether and the solid filtered, washed with pentane and dried. Finally,a portion of this solid (crude 7-iodo-quinolin-4-ol, 7, 0.50 g, 1.8 mmol) was reacted with phosphorus oxychloride (5 mL)at 130 °C for 2.5 hours. The excess POCl3 was removed under reducedpressure and the resulting oily residue treated with an ice-cold concentratedammonia solution. After extracting with dichloromethane (2 x 20 mL), theorganic layers were combined, dried over anhydrous magnesium sulphate andfiltered. The brownish solid obtained after removing solvents was purified bycolumn chromatography over silica gel eluting with petroleum ether/ethylacetate 20:1, then 10:1 to furnish pure 8as white crystals in 38 percent overall yield. 1H-NMR (500 MHz, CDCl3)delta in ppm: 7.47 (d, 3J=4.7Hz, 1H, H3), 7.87 (dd, 3J=8.9Hz, 4J=1.4 Hz, 1H, H6),7.91 (d, 3J=8.9 Hz, 1H,H5), 8.53 (d, 4J=1.4 Hz,1H, H8), 8.75 (d, 4J=4.7Hz, 1H, H2). 13C-NMR (125 MHz, CDCl3) delta in ppm: 97.0, 121.8 (CH), 125.4 (CH), 125.8, 136.5(CH),138.8 (CH), 143.0, 149.7, 150.7 (CH). HRMS-FAB [M+]: m/z288.9142 (calculated for C9H5NClI 288.9149). |
Tags: 22297-71-8 synthesis path| 22297-71-8 SDS| 22297-71-8 COA| 22297-71-8 purity| 22297-71-8 application| 22297-71-8 NMR| 22297-71-8 COA| 22297-71-8 structure
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