Electric Literature of 4863-91-6, In the chemical reaction process, reaction time, type of solvent, can easily affect the result of the reaction, thereby determining the yield and properties of the reaction product. An updated downstream synthesis route of 4863-91-6 as follows.
Example 9: Synthesis of Compound 38 Compound 38 [0111] A flame-dried flask was charged with 5-chlorobenzo[c][l,2,5]oxadiazole (100.0 mg, 0.65 mmol, 1 equiv) and toluene (3mL), and the mixture was stirred at 1 10 C for 30 min with a reflux condenser. The solution was cooled to room temperature, and the flask was charged sequentially with palladium (II) acetate (8.8 mg, 0.040 mmol, 6 mol%), racemic 2,2′- bis(diphenylphosphino)-l, l’-binaphthyl (24.9 mg, 0.040 mmol, 6 mol%), 2-chloro-4- fluoroaniline (68.4 mu,, 0.65 mmol, 1 equiv) and potassium tert-butoxide (80.0 mg, .71 mmol, 1.1 equiv). The mixture was stirred at 90 C for 12 h, cooled to room temperature, and diluted with water. The mixture was washed with dichloromethane (3x). The combined organic layers were washed with IN HC1, IN NaOH, and brine. The organic layers were then dried over MgS04 and concentrated under reduced pressure. The resulting solid was then recrystallized in hexanes to provide compound 38 as a brown solid (67 mg, 39% yield): XH NMR (400 MHz, Acetone-d6) 8.59 (bs, 1H), 7.87 (d, J = 9.2 Hz, 1H), 7.40 (dd, J= 2.0 Hz, 9.6 Hz, 1H), 7.31 (m, 1H), 7.20 (s, 1H), 7.12 (dt, J= 1.3 Hz, 12.0 Hz, 1 Hz), 6.92 (dt, J= 2.0 Hz, 8.6 Hz, 1H); 13C NMR (100 MHz, Acetone-d6) 164.4 (d, J = 245.3 Hz), 151.1, 147.9, 145.4, 144.9 (d, J = 1 1.9 Hz), 136.3 (d, J = 13.2 Hz), 131.0, 118.2, 1 16.3, 1 10.6 (d, J = 25.5 Hz) 105.9 (d, J= 25.0 Hz), 91.7; LCMS (ESI) calc’d for [Ci2H6ClFN30]”([M-H]”): m/z 262.0, found 262.0.
According to the analysis of related databases, 4863-91-6, the application of this compound in the production field has become more and more popular.
Reference:
Patent; THE BOARD OF REGENTS OF THE UNIVERSITY OF TEXAS SYSTEM; BRUICK, Richard, K.; CALDWELL, Charles, G.; FRANTZ, Doug, E.; GARDNER, Kevin, H.; MACMILLAN, John, B.; SCHEUERMANN, Thomas, H.; TAMBAR, Uttam, K.; WO2014/78479; (2014); A2;,
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