Arylamine derivative, preparation method and application thereof
A technology of derivatives and aromatic amines, applied in the field of organic electroluminescent devices
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[0087] The application also provides the preparation method of the arylamine derivative, specifically:
[0088] reacting the compound having the structure of formula (IV) with the compound having the structure of formula (V) under the action of a catalyst and an alkali metal salt to obtain an arylamine derivative having the structure of formula (I);
[0089]
[0090]
[0091] Among them, X 1 、X 2 independently selected from N-Ar 1 , O, S or SO 2 ;
[0092] R 1 ~R 8 Each independently selected from hydrogen, deuterium, halogen, cyano, hydroxyl, nitro, substituted or unsubstituted C1~C20 alkyl, substituted or unsubstituted C6~C30 aryl, substituted or unsubstituted C2~ C30 heteroaryl, substituted or unsubstituted C1-C20 alkoxy, substituted or unsubstituted C6-C20 aryloxy, substituted or unsubstituted C3-C40 silyloxy, substituted or unsubstituted C1-C20 acyl, substituted or unsubstituted C2-C20 alkoxycarbonyl, substituted or unsubstituted C2-C20 acyloxy, substituted...
Embodiment 1
[0108]
[0109] In a nitrogen atmosphere, 10.0 g (10.9 mmol) of intermediate M-3-1-1, 3.15 g (13.08 mmol) of 2-chloro-4-phenylquinazoline and 0.27 g of 0.27 g (0.22 mmol) ) of tetrakis (triphenylphosphine) palladium is put into a flask and dissolved in a mixed solvent of 250ml of toluene, ethanol and water (volume ratio 3:1:1); then, the aqueous solution of potassium carbonate of 6g (43.6mmol) Add in the above reactant, then reflux and stir for 12 hours, after the reaction, extract the reactant with ethyl acetate; dry the extracted product with magnesium sulfite and filter, then, concentrate and filter the product under reduced pressure, use silica gel column chromatography (developing Agent ratio: petroleum ether / dichloromethane=3:1) to purify the concentrated product to obtain 9.4g of compound 28 (yield=87%), mass spectrum: theoretical value: 995.31; measured value: 995.32.
Embodiment 2
[0111]The same preparation method as in Example 1, the difference is that 2-chloro-4-phenylquinazoline is replaced by 4-bromobiphenyl to obtain 8.74g of compound 80 (yield=85%), mass spectrum: theoretical value : 943.31; The measured value is 943.33.
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