A kind of bifunctional complexing agent containing tetraphenylethylene and its preparation method and application
A tetraphenylethylene and bifunctional technology, which is applied in the field of organic bifunctional complexing agent synthesis, can solve the problems of affecting target binding and large synthesis workload, and achieves the effects of simple synthesis conditions, easy operation and mild reaction conditions.
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[0042] The synthetic method of above-mentioned bifunctional complexing agent containing tetraphenylethylene specifically comprises the steps:
[0043] 1)
[0044] Under anhydrous conditions, dissolve an equimolar amount of o-hydroxybenzoyl tetraphenylethylene derivatives or o-hydroxybenzoyl derivatives in dichloromethane, chloroform or methanol, and add half the mole of the initial aldehyde group The amount of ethylenediamine, and then react at 0-80°C for 3-12h;
[0045] 2) Reduction of Schiff base
[0046] Add solvent ethanol or methanol or tetrahydrofuran to the product obtained in step 1), then add a reducing agent twice the molar amount of the initial raw material, and react for 10 minutes;
[0047] 3) Purification of imines
[0048] Use dilute hydrochloric acid with a concentration of 1-3mol / L as a neutralizing agent for neutralization, then add ethyl acetate for extraction, dry over anhydrous sodium sulfate, remove the solvent with a vacuum rotary evaporator, and perf...
Embodiment 1
[0054] 2,2'-(Ethane-1,2-diylbis((2-hydroxy-5-(1,2,2-triphenylethenyl)benzyl)azadiyl))diacetic acid
[0055] structural formula
[0056]
[0057] Reaction formula
[0058]
[0059] Synthesis of raw materials:
[0060] 2-Hydroxy-5-(1,2,2-triphenylvinyl)benzaldehyde, the structural formula is as follows:
[0061]
[0062] References 2017 Tetrahedron Letters, 58(20), 1980-1984;
[0063] 2,2'-((ethane-1,2-diylbis(azanediyl))bis(methylene))bis(4-(1,2,2-triphenylethenyl)phenol) , the structural formula is as follows:
[0064]
[0065] Reaction formula:
[0066]
[0067] A solution of 2-hydroxy-5-(1,2,2-triphenylethenyl)benzaldehyde (0.69 g, 2 mmol) was added to 20 ml of methanol at room temperature, and ethane-1,2-diamine ( 60 mg, 1 mmol). The solution was kept at room temperature at 60°C for 3 hours. NaBH at 0°C 4 (0.14g, 4mmol) was added to the solution in batches and reacted for 10 minutes. The reaction was then acidified to pH = 7 with 1M HCl while coolin...
Embodiment 2
[0078] 2,2'-tert-butyl-(ethane-1,2-diylbis((2-hydroxy-5-(1,2,2-triphenylethenyl)benzyl)azadiyl)) Diglutaric acid, the structural formula is as follows:
[0079]
[0080] Reaction intermediate: 2,2'-(ethane-1,2-diylbis((2-hydroxy-5-(1,2,2-triphenylethenyl)benzyl)azadiyl)di Dimethyl acetate
[0081] The structural formula is as follows:
[0082]
[0083] The reaction formula is as follows:
[0084]
[0085] The compound 2,2'-((ethane-1,2-diylbis(azanediyl))bis(methylene))bis(4-(1,2,2-triphenylethenyl) Phenol) (0.4g, 0.51mmol) and K 2 CO 3 (0.28g, 2mmol) solution was added in 45mL acetonitrile, stirred at room temperature for 0.5 hours, 1-(tert-butyl) 5-methyl 2-bromoglutaric acid ester (280mg, 1mmol) was added, and then reacted at 60 Stir overnight at °C. The reaction was filtered and evaporated in vacuo, purified with flash purifier (hexane / ethyl acetate=4 / 1) to give 2,2'-(ethane-1,2-diylbis((2-hydroxy-5- Dimethyl (1,2,2-triphenylethenyl)benzyl)azadiyl)diacetat...
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