36 results about "Ugi reaction" patented technology

The invention provides a functionalized nano-grade porous polymer material multicomponent reaction preparation method comprising the following steps: a, an aldehyde reactant comprising double bond is prepared through multicomponent synthesis; b, a Ugi four-component reaction is realized with 4-allyloxylbenzaldehyde prepared in the step a, such that a functional monomer is obtained; and c, divinyl benzene is adopted as a crosslinking monomer; an initiator is added; and divinyl benzene is subjected to a copolymerization reaction with a proper amount of the Ugi reaction product with a solvothermal method, such that the functionalized nano-grade porous polymer material is obtained. A mass ratio of divinyl benzene to the functional monomer is 1.0-4.0. A mass ratio of the initiator to divinyl benzene is 0.01-0.05. A mass ratio of the solvent to divinyl benzene is 4.0-10.0. The polymerization temperature is within a range of 60-200 DEG C. The pressure is controlled at 0.5-5.0MPa. The reaction time is 24-48h. After the reaction, residual solvent is removed through room-temperature volatilization or reduced-pressure distillation.

The invention relates to a preparation method and application of carbazole derivatives. On the basis of a four-component Ugi reaction, the carbazole derivatives are synthesized through cyclization ofsynthesized intermediates by a microwave assisted reaction in a DMF (dimethyl formamide) solvent on the basis of no purification. The carbazole derivatives have antitumor activity.

The invention relates to the field of biopolymer materials and particularly relates to a modified polymannuronic acid derivative, a drug-carrying aqueous emulsion and a preparation method thereof. Low-molecular-weight polymannuronic acid as a raw material undergoes an Ugi reaction to produce an amphiphilic polymannuronic acid derivative. The surface activity test result shows that the derivative has a low critical aggregation concentration and good surface activity, can be used as a water emulsion stability aid and has a good regulation effect on the stability and drug release of the emulsion.

The invention relates to an quinoxaline-azetidinones compound preparation and an application of the quinoxaline-azetidinones compound in tumor resistance. According to the invention, a Ugi reaction is taken as a base, under microwave assistance, azetidinone is obtained through ring closure under diisopropylamine condition, then quinoxaline ring is obtained in a trifluoroacetic acid / dichloroethanes solution with concentration of 10%, and the quinoxaline-azetidinones compound has latent antitumor activity.

The invention relates to flame retardants containing melamine structure as well as a preparation method and application thereof. The chemical structural formula of the flame retardants is shown in thedescription, wherein substituent groups R1, R2 and R3 are any one of hydrogen, tertiary butyl, normal-butyl, cyclohexyl alkyl or chlorine, bromine, methyl, methoxy, nitryl, amino, hydroxy-substitutedaryl or ceteroary. A synthesis method comprises the following steps: carrying out Ugi reaction on carboxylic acid compounds, the melamine, aldehyde compounds and isonitrile compounds in a mixed solvent of methanol and isopropanol at the temperature of 50 DEG C under the concerted catalysis of an MCM-41-loaded copper complex, MIL-101 and p-toluenesulfonic acid; carrying out filtering, extracting and column chromatography on a product to obtain the flame retardants containing the melamine. The invention discloses a novel preparation method with the advantages of simple reaction, few byproductsand better selectivity, which is used for selectively synthesizing the melamine flame retardants. The flame retardants disclosed by the invention have the advantages of good thermal stability, high flame retardancy rate, high purity reaching to 97.2 percent, easily-obtained raw materials, advanced technology and easiness for industrial production.

The invention discloses a preparation method of N-(indole-N-formyl)-α-aminoamide derivatives, which comprises the following steps: N-indole carboxylic acid compounds, aldehyde compounds, primary amine compounds and The four-component reaction of the isonitrile compound in the solvent; or the three-component reaction of the N-indole carboxylic acid compound, the cyclic imine compound and the isonitrile compound in the solvent. After the reaction is completed, the post-treatment obtains the N-(indole-N-formyl)-α-aminoamide derivative; the preparation method uses the indole compound as a potential component of the classic Ugi reaction, in mild The rapid connection of indole skeleton and α-aminoamide is realized under the conditions, the reaction is efficient, concise and fast, and the yield is high, which has far-reaching significance for organic synthesis and medicinal chemistry.

The invention relates to a preparation method of a benzodiazepine compound, which comprises the following steps: reacting amino functionalized ionic liquid, phenylpropyl aldehyde, Boc-anthranilic acid and cyclohexyl isonitrile to obtain an ionic-liquid-loaded Ugi product; reacting the ionic-liquid-loaded Ugi product under the catalytic action of hydrogen chloride gas to obtain a benzodiazepine compound of which the side chain is modified by Ugi reaction; and carrying out rotary evaporation on the reaction liquid, and washing out residues with anhydrous aether to obtain the required benzodiazepine compound. Compared with the existing preparation method, the preparation method provided by the invention shortens the reaction procedures and enhances the reaction efficiency; and the synthesis method is simple and efficient, and has wide application prospects.

The invention provides an amino acid based clustering peptide and a preparation method thereof and belongs to technical field of high polymer chemistry. The problem that an existing clustering peptide synthesis method is complicated in process, long in reaction cycle and restricted in practical application is solved. The structure of the amino acid based clustering peptide is shown as a formula I. The invention further provides the preparation method of the amino acid based clustering peptide. According to the method, amino acid or an amino acid derivative, aldehyde and fenvalerate are mixed in an organic solvent to obtain the amino acid based clustering peptide. The amino acid based clustering peptide is synthesized through Ugi reaction, the reaction conditions are mild, no catalyst is needed, the preparation process is simple, a reaction period is short, and experimental results show that the amino acid based clustering peptide with the concentration of 10 micro-g mL-1 to 100 micro-g mL-1 has a very good inhibiting effect on staphylococcus aureus, is superior to currently commercial epsilon-polylysine and has a good application prospect.

The invention relates to a preparation method and application of a condensed benzimidazole azetidinone derivative. The method comprises the steps of performing ring closure into azetidinone under an alkaline condition based on a Ugi reaction, and then obtaining a benzimidazole ring under an acidic condition. The condensed benzimidazole azetidinone derivative has potential anti-tumor activity.