Compound and application thereof, and organic electroluminescent device comprising compound
A compound, unsubstituted technology, applied in the field of organic electroluminescent devices, can solve the problems of OLED product efficiency, lifespan, cost, etc. that cannot be completely resolved, and achieve the effects of high efficiency and lifespan, reduced driving voltage, and improved efficiency and lifespan
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Synthetic example 1
[0174] Synthesis Example 1: Synthesis of Compound P4
[0175]
[0176] (1) 2-chloro-4-phenylquinazoline (30mmol), intermediate M1 (30mmol), three (dibenzylideneacetone) dipalladium (0.30mmol), tri-tert-butylphosphorus toluene solution (0.30 mmol), sodium tert-butoxide (60mmol), xylene (300mL), heated to 100°C for 12h under nitrogen protection, the reaction was completed by TLC monitoring, and the reaction liquid was concentrated and separated by column chromatography to obtain intermediate P4-A.
[0177]
[0178] (2) Intermediate P4-A (25mmol), 9,9-dimethylacridine (25mmol), tris(dibenzylideneacetone) dipalladium (0.25mmol), tri-tert-butylphosphonium toluene solution (0.25 mmol), sodium tert-butoxide (50mmol), xylene (300mL), were added to the reaction flask, heated to reflux reaction for 12h under nitrogen protection, TLC monitored the completion of the reaction, the reaction solution was cooled and filtered, and the filter cake was washed with ethanol to obtain the com...
Synthetic example 2
[0180] Synthesis Example 2: Synthesis of Compound P15
[0181] The difference from Synthesis Example 1 is that 2-chloro-4-phenylquinazoline is replaced by 2-chloro-4,6-diphenyl-1,3,5-triazine of the same amount, and the intermediate Substitution of intermediate M1 by an equivalent amount of intermediate M2 affords compound P15.
[0182] MS: C 46 h 33 N 5 , theoretical value: 655.27, actual value: 656.28.
Synthetic example 3
[0183] Synthesis Example 3: Synthesis of Compound P26
[0184]
[0185] (1) 2-chloro-4-phenylquinazoline (30mmol), p-fluorophenylboronic acid (30mmol), tetrakis (triphenylphosphine) palladium 0.3mmol, potassium carbonate (60mmol), 1,4-diox Hexacyclic (300mL) and 60mL of water were added to the reaction flask, heated to 120°C for 5h under the protection of nitrogen, and the reaction was monitored by TLC. The reaction solution was poured into water for filtration, and the filter cake was washed with ethanol to obtain intermediate P26-A.
[0186]
[0187] (2) Add intermediate P26-A (30mmol), intermediate M3 (30mmol), cesium carbonate (60mmol), DMF (300mL) into the reaction flask, heat to reflux reaction for 12h under the protection of nitrogen, and monitor the completion of the reaction by TLC , Pour the reaction solution into water to filter, and wash the filter cake with ethanol to obtain the intermediate P26-B.
[0188]
[0189] (3) Same as step (2) in Synthesis Exam...
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