Organic compound taking triazine and benzimidazole as cores and application thereof
An organic compound, benzimidazole technology, applied in the field of organic compounds and its application in OLED, can solve the problems of complex manufacturing process and affecting the angular distribution of OLED radiation spectrum
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Embodiment 1
[0056] Embodiment 1: the synthesis of intermediate I
[0057] When Ar 1 When it is a single key,
[0058]
[0059] Weigh raw materials 2,4,6-trichloro-1,3,5-triazine and R 1 -H, dissolve in toluene; then add Pd 2 (dba) 3 , tri-tert-butylphosphine, sodium tert-butoxide; under an inert atmosphere, react the mixed solution of the above reactants at a reaction temperature of 95-110°C for 10-24 hours, cool and filter the reaction solution, spin the filtrate, and pass through silica gel Column, obtain intermediate I;
[0060] The 2,4,6-trichloro-1,3,5-triazine and R 1 The molar ratio of -H is 1:1.0~1.5, Pd 2 (dba) 3 The molar ratio to 2,4,6-trichloro-1,3,5-triazine is 0.006~0.02:1, tri-tert-butylphosphine and 2,4,6-trichloro-1,3,5-triazine The molar ratio of oxazine is 0.006~0.02:1, and the molar ratio of sodium tert-butoxide to 2,4,6-trichloro-1,3,5-triazine is 2.0~3.0:1;
[0061] When Ar 1 When not a single key,
[0062]
[0063] Under nitrogen atmosphere, weigh R...
Embodiment 2
[0082] Embodiment 2: intermediate Synthesis
[0083] When Ar 2 or Ar 3 When expressed as a structure of general formula (3),
[0084]
[0085] (1) In a 250mL three-necked flask, feed nitrogen, add 0.02mol raw material 2-bromo-benzimidazole, 0.03mol iodobenzene, 0.04mol sodium hydride, 0.004mol cuprous iodide and 0.01mol o-phenanthroline and dissolve in In 100ml 1,3-dimethyl-2-imidazolidinone, stir the reaction for 20-30h, after the reaction, add water and extract with dichloromethane, dry the organic layer with anhydrous sodium sulfate, and use petroleum ether and ethyl acetate The mixture was rinsed with eluent, the volume ratio of petroleum ether and ethyl acetate in the eluent was 1:100, and purified by column chromatography to obtain intermediate M;
[0086]
[0087] (2) Under a nitrogen atmosphere, weigh the intermediate M and dissolve it in tetrahydrofuran, and then dissolve the Br-Ar 2 -B(OH) 2 And tetrakis (triphenylphosphine) palladium is added, the mixtu...
Embodiment 3
[0120] Embodiment 3: the synthesis of compound 1:
[0121]
[0122] In a 250mL three-neck flask, blow nitrogen, add 0.01mol intermediate A1, 150ml DMF, 0.03mol intermediate B1, 0.0002mol palladium acetate, stir, and then add 0.02mol K 3 PO 4 The aqueous solution was heated to 150°C, refluxed for 24 hours, sampled and plated, and the reaction was complete. Cool naturally, extract with 200ml of dichloromethane, separate layers, dry the extract with anhydrous sodium sulfate, filter, rotate the filtrate, and purify through a silica gel column to obtain the target product with a HPLC purity of 99.2% and a yield of 65.4%.
[0123] Elemental analysis structure (molecular formula C 59 h 40 N 8 ): theoretical value C, 82.30; H, 4.68; N, 13.01; test value: C, 82.30; H, 4.67; N, 13.03. ESI-MS(m / z)(M + ): The theoretical value is 860.34, and the measured value is 860.64.
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