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77 results about "Phenyl hydrazine" patented technology

Preparation method and application of pH sensitive drug delivery system with carbon nanomaterial as carrier

The invention relates to a preparation method and application of a pH sensitive drug delivery system with a carbon nanomaterial as a carrier. The pH sensitive drug delivery system can be used for effectively solving the problems that the traditional tumor therapy drugs are high in side effect and incapable of well inhibiting the tumor cell proliferation. The technical scheme for solving the problems is as follows: the preparation method comprises the following steps of: modifying the original carbon nanomaterial, and then, subjecting the modified original carbon nanomaterial and an ammoniation reagent to a reaction; after connecting an amino with reaction activity to the surface of the carbon nanomaterial, subjecting the carbon nanomaterial and p-hydrazinobenzoic acid to a reaction to generate a p-hydrazinobenzoic acid derivative of the carbon nanomaterial; and then, subjecting the p-hydrazinobenzoic acid derivative and a carbonyl contained anti-tumor drug to a reaction to obtain the pH sensitive drug delivery system with the carbon nanomaterial as the carrier, wherein the carbon nanomaterial is one selected from fullerene, a carbon nanotube and graphene oxide. The pH sensitive drug delivery system is good in biocompatibility, large in specific surface area and high in chemical inertness, has a control release feature and a targeting property, and is an innovation of the anti-tumor drug.
Owner:ZHENGZHOU UNIV

Phenyl hydrazine and substituted phenyl hydrazine continuous flow synthesis process

ActiveCN107663161ARealize the whole process of continuous flow synthesisSolve the technical problems of continuous production in the whole processHydrazine preparationSequential/parallel process reactionsReaction intermediateDiazoamino Compounds
The invention provides a phenyl hydrazine and substituted phenyl hydrazine continuous flow synthesis process. Three-step reactions of diazotization, reduction and acidolysis salt formation are creatively and organically integrated; phenylamine or substituted phenylamine acid material liquid, diazotization reagents, reducing agents and acid are used as raw materials to be subjected to three-step reaction of diazotization, reduction and acidolysis salt formation to obtain phenyl hydrazine derivative salts. The synthesis process is performed in an integral reactor, and belongs to an integrated solution. The reaction raw materials are continuously added through a feeding opening of the integral reactor; the reactions of diazotization, reduction and acidolysis salt formation are continuously performed in the integral reactor; the phenyl hydrazine derivative salts are continuously obtained in the integral reactor; the total reaction time is less than or equal to 20min. Compared with a conventional production process, the continuous flow synthesis process has the advantages that the total reaction time is greatly shortened; the safety is greatly improved; no reaction byproducts (such as diazoamino compounds and reduction reaction midbodies) are included in the reaction process and the reaction products; the continuous flow process can prepare the high-purity products with the purity as high as 99 percent or higher without the additional purification steps.
Owner:SHANGHAI HYBRID CHEM TECH

Synthesis method of para-trifluoromethyl phenyl hydrazine hydrochloride

The invention relates to a synthesis method of para-trifluoromethyl phenyl hydrazine hydrochloride, which comprises the following steps: firstly leading para-trifluoromethylaniline and sodium nitrite to carry out diazotization reaction: adding concentrated hydrochloric acid and water into a four-neck flask, and starting stirring; dripping the para-trifluoromethylaniline, generating a larger number of white solids, and controlling the temperature at -5 DEG C-15 DEG C; reducing the temperature to -5 DEG C-5 DEG C, dripping sodium nitrite solution, controlling the temperature at -5 DEG C-15 DEG C, dripping 10-12% of sodium carbonate solution, and adjusting the pH value of diazotization reaction solution to 5-7; further carrying out reduction reaction: adding sodium sulfite solution into the four-neck flask, reducing the temperature to 0-20 DEG C and starting stirring; dripping the diazotization reaction solution into the sodium sulfite solution in batches, keeping the temperature at 0-25 DEG C, and stirring at the room temperature for 1-3h; adding the concentrated hydrochloric acid, and carrying out heating reflux for 1-4h; and reducing the temperature to 0 DEG C-20 DEG C, filtering, drying, and obtaining the para-trifluoromethyl phenyl hydrazine hydrochloride. The yield is greater than 75% and the purity is 97%-99%.
Owner:大连凯飞精细化工有限公司

Method of using deep eutectic solvent to prepare 2-arylindole compounds

The invention discloses a method of using a deep eutectic solvent to prepare 2-arylindole compounds, and relates to the technical field of organic compound preparation. The deep eutectic solvent is environment-friendly and is taken as the reaction solvent and catalyst. 2-arylindole compounds are prepared through one-step reactions between phenyl hydrazine and substituted acetophenone. The method comprises the following steps: mixing choline chloride (ChCl) and zinc chloride (ZnCl2) according to a mole ratio of 1:4, slowly heating to a temperature of 95 to 100 DEG C, maintaining the temperature, stirring the mixture by magnetic force for 8 to 12 hours to obtain a deep eutectic solvent (ChCl+4ZnCl2); sequentially adding the prepared deep eutectic solvent, phenyl hydrazine, and substituted acetophenone into a reactor according to a mole ratio of 1:1:1, magnetically stirring the mixture for 70 to 90 minutes at a temperature of 120 to 125 DEG C, after reactions, cooling to the room temperature, adding water, stirring, carrying out vacuum suction filtration, washing the filter cake by polyphosphoric acid (10%) until the filter cake becomes neutral to obtain a coarse product, and further recrystallizing the coarse product by ethanol (95%) to obtain a pure crystalline product. The synthesis method is simple, the raw materials are easily available, the cost is low, and the method can be applied to massive production.
Owner:XINZHOU TEACHERS UNIV
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