Compound containing pyrido indole, and applications in organic electroluminescent devices
A compound and electroluminescent technology, applied to organic electroluminescent devices, in the field of compounds containing pyrido indole, can solve problems such as disparity, and achieve the effects of not easy aggregation, balanced distribution, and improved compound efficiency
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Embodiment 1
[0051] Embodiment 1: the synthesis of intermediate M:
[0052]
[0053] (1) Dissolve raw material B and raw material C in a mixed solution of toluene and ethanol, add Pd(PPh 3 ) 4 and K 2 CO 3 , react at 95-110°C for 10-24 hours under an inert atmosphere, monitor the reaction process with TLC during the reaction process, cool and filter the raw materials after the reaction is complete, spin the filtrate to remove the solvent, and pass the crude product through a silica gel column to obtain Intermediate S;
[0054] Wherein, the consumption of described toluene and ethanol is to use 30~50mL toluene and 5~10mL ethanol per gram of raw material C, the molar ratio of raw material B and raw material C is (1~1.5):1, Pd(PPh 3 ) 4 The molar ratio with raw material C is (0.006~0.02):1, K 2 CO 3 The molar ratio with raw material C is (1.5~2):1.
[0055] (2) Under the protection of nitrogen, weigh 0.01mol of intermediate S and dissolve it in 150mL tetrahydrofuran, cool to -78°C,...
Embodiment 2
[0065] Embodiment 2: the synthesis of compound 2:
[0066]
[0067] In a 250mL three-necked flask, dissolve 0.01mol of raw material A-1 and 0.012mol of raw material B-1 in 150mL of toluene and ethanol (V 甲苯 :V 乙醇 =5:1) In the mixed solution, add 0.0002mol Pd(PPh 3 ) 4 and 0.02mol K 2 CO 3 , reacted at 110°C for 24 hours under an inert atmosphere, and continuously monitored the reaction process with TLC during the reaction process. After the raw materials were completely reacted, cooled and filtered, the filtrate was rotary evaporated to remove the solvent, and the crude product was passed through a silica gel column to obtain the target product; element Analytical structure (molecular formula C 42 h 28 N 2 ): theoretical value C, 89.97; H, 5.03; N, 5.00; test value: C, 89.98; H, 5.07; N, 5.01; for 560.27.
Embodiment 3
[0068] Embodiment 3: the synthesis of compound 15:
[0069]
[0070] In a 250mL three-necked flask, dissolve 0.01mol of raw material A-2 and 0.012mol of raw material B-3 in 150mL of toluene and ethanol (V 甲苯 :V 乙醇 =5:1) In the mixed solution, add 0.0002mol Pd(PPh 3 ) 4 and 0.02mol K 2 CO 3 , reacted at 110°C for 24 hours under an inert atmosphere, and continuously monitored the reaction process with TLC during the reaction process. After the raw materials were completely reacted, cooled and filtered, the filtrate was rotary evaporated to remove the solvent, and the crude product was passed through a silica gel column to obtain the target product; element Analytical structure (molecular formula C 42 h 28 N 2 ): theoretical value C, 89.97; H, 5.03; N, 5.00; test value: C, 89.98; H, 5.08; N, 5.07; for 560.28.
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