43 results about "O-fluoronitrobenzene" patented technology

The invention concerns the reaction of benzene catalyst adding hydrogen, specific speaking, it's a kind of catalyst to produce 4-ammonia base-3-F benzene fen and its application. The catalyst is made of carrier, active parts and helping dose. The main active parts are: dear metal Pt, Pd or Rh, whose weight is of catalyst 0.1%--20%. Help doses are IA, ó�A, ó¾B, ó° or Sparse soil chemical element. The catalyst has the feature of high active in reactivation, good choosing ability and many reuses. The catalyst can also be used in other replacing nitric unit benzene adding hydrogen and catalyst process.

The present invention relates to the field of organic synthesis, in particular to a preparation method of 2-methoxy-5-bromoaniline, which uses o-fluoronitrobenzene as a raw material, and undergoes three-step finishing synthesis of bromination, etherification and reduction reactions to obtain a medicine Intermediate 2-methoxy-5-bromoaniline. 2-Methoxy-5-bromoaniline is an important fine chemical intermediate and has a wide range of uses in the pharmaceutical industry. At present, there are few reports on related synthesis methods, and none of them are suitable for industrial production. The invention relates to a preparation method of 2-methoxy-5-bromoaniline. The method uses o-fluoronitrobenzene as a raw material, and undergoes three steps of bromination, etherification and reduction to obtain the pharmaceutical intermediate 2-methoxy-5-bromoaniline, with a total yield of 67.7%. The method of the invention has cheap raw materials and mild reaction conditions, and opens up a process for synthesizing 2-methoxy-5-bromoaniline.

The invention discloses a method for preparing o-fluoroaniline by hydrogenating o-fluoronitrobenzene. The method comprises the following steps: 1, filling a fixed bed reactor with a catalyst, introducing air and heating; 2, uniformly mixing o-fluoronitrobenzene steam and preheated hydrogen to obtain mixed gas, introducing the mixed gas into the fixed bed reactor, and performing a catalytic hydrogenation reaction in the presence of the catalyst; and 3, delivering the material subjected to the catalytic hydrogenation reaction into a condenser, condensing the material to convert the o-fluoronitrobenzene steam in the material into a liquid state, and separating the liquid-state o-fluoronitrobenzene in an oil-water separator to obtain oil-state o-fluoroaniline. The o-fluoronitrobenzene is catalytically hydrogenated by adopting the method, the treatment amount is large, the o-fluoronitrobenzene is completely converted, the molar conversion rate of the o-fluoronitrobenzene is 100 percent, and the molar percentage of a defluorinated product is less than 0.1 percent; and the product separating and purifying operation is simple at low energy consumption, and no toxic or harmful ions are doped in the product.

The invention discloses a method for separating and comprehensively utilizing nitrobenzene chlorides, which comprises the separation and comprehensive utilization of monochloride and the comprehensive utilization of dichloride, wherein the monochloride is subjected to fluorine substituted reaction to separate m-nitrochlorobenzene, o-fluoronitrobenzene and dinitro-fluorobenzene, and the o-fluoronitrobenzene and the dinitro-fluorobenzene are taken as products for sale, or a mixture is subjected to chlorination to generate 2,4-dichlor fluorbenzene with higher economic value; and the dichloride is subjected to chlorination to generate the 2,4-dichlor fluorbenzene with higher economic value. The method improves the yield of the m-nitrochlorobenzene on the one hand, and utilizes the resources with low economic value to produce the product with higher economic value by steps of reasonable chemical reaction and separation, brings economic benefit to enterprises and solves environmental pollution problem on the other hand.

The invention relates to a preparation method of an antipsychotic drug olanzapine. The method comprises three steps: first, using sulfur, propionaldehyde and malononitrile as raw materials, triethylamine as a catalyst to carry out ringclosure to obtain 5-methyl-2-amino-3-cyanothiophene; second, the 5-methyl-2-amino-3-cyanothiophene and o-fluoronitrobenzene generating 5-methyl-2-(2- nitrophenylamino)-3-cyanothiophene under effects of sodium hydride; third, the 5-methyl-2-(2- nitrophenylamino)-3-cyanothiophene reacting with hydrazine hydrate and N-methyl piperazine to carry out ringclosure reaction under existence of ferric trichloride / active carbon catalyst; so as to generate objective compound olanzapine through a one-pot method. The invention has the advantages of cheap and easily available raw materials, few steps, and simple process. A one-pot reaction is carried out in the third step, so that intermediate state compounds during the reaction process do not need to be separated or removed and can converse into the objective compound, and the high-purity olanzapine can be obtained with high yield. The whole process is suitable for industrial mass production with high product yield, low costs and convenient post-treatment.

The invention discloses a method of comprehensively use of chloronitrobenzene mixture by fluoro-reaction, comprising steps of: generating a mixture mainly composed of parachloronitrobenzene, o-chloronitrobenzene and m-chloronitrobenzene in process of parachloronitrobenzene, o-chloronitrobenzene by chlorobenzene nitration method; removing low-boiling-point substances by evaporation; then adding anhydrous potassium fluoride and catalyst to the mixture for fluoro-reaction at 150 DEG. C to 250 DEG. C; after reaction, filtering to remove potassium chloride, after rectifying to acquire parachloronitrobenzene, o-chloronitrobenzene, the residual portion via recrystallization acquires m-chloronitrobenzene; the catalyst is quaternary ammonium salt or calixarene; charge rate of chloronitrobenzene mixture and mixture is 1:0.01 to 1. The method of the invention is simple to operate, in scale and changes waste material into things of value, which realizes zero discharge. The method is characterizedin sustainable development, energy saving, consumption reduction and environmentally friendly property.

The invention provides a method for synthesizing N-(4-chlorphenyl)-1,2-phenylenediamine as a key clofazimine intermediate. The method specifically comprises the following steps: 1) by taking o-fluoronitrobenzene and p-chloroaniline as raw materials and utilizing organic base as a catalyst for condensation reaction, reacting in an organic solvent and performing conventional treatment after ending the reaction, thereby acquiring a condensation intermediate N-(4-chlorphenyl)-2-nitryl-1-aniline; 2) by utilizing metallic nickel as the catalyst, performing catalytic hydrogenation reaction on the acquired condensation intermediate in the organic solvent and performing conventional treatment after reducing, thereby acquiring a rough product of N-(4-chlorphenyl)-1,2-phenylenediamine; and 3) re-crystallizing the acquired rough product with the organic solvent, thereby acquiring the end product.

The invention relates to a synthetic route for preparing olanzapine by using o-fluoro-nitrobenzene as a raw material. In the method, the o-fluoro-nitrobenzene is used as a starting material to prepare the olanzapine by steps of coupling, reduction and ring closing.

The present invention relates to the field of pharmaceutical chemistry, to a preparation method of a new intermediate of 5-chloro-N2-(2-isopropoxy-5-methyl-4-(piperidine-4-yl)phenyl)-N4-(2-(isopropylsulfonyl)phenyl)pyrimidine-2,4-diamine (Ceritinib). According to the present invention, o-fluoronitrobenzene is adopted as a starting raw material, substitution, reduction and condensation are performed to obtain the new intermediate 2-X-5-chloro-N-(2-(isopropyl sulfide)phenyl)pyrimidine-4-amine (X is halogen, p-methyl benzene sulfonyloxy, methyl sulfonyloxy or trifluoromethylsulfonyloxy), the new intermediate can be oxidized to obtain a sulfonyl derivative, and the sulfonyl derivative and 2-isopropoxy-5-methyl-4-(piperidine-4-yl)aniline are subjected to condensation to finally obtain 5-chloro-N2-(2-isopropoxy-5-methyl-4-(piperidine-4-yl)phenyl)-N4-(2-(isopropylsulfonyl)phenyl)pyrimidine-2,4-diamine (Ceritinib); and the synthesis method has characteristics of readily available raw materials, high yield, mild reaction, simple operation and low production cost, and is suitable for industrial production.

The invention relates to a new process for producing 4-amino-3-fluorophenol, which takes o-fluoronitrolbenzene as raw material and platinum-carbon or palladium-charcoal as a catalyst and adopts hydrogen pressure reaction to produce the 4-amino-3-fluorophenol in an acidic aqueous solution which contains organic solvents. The production technology is simpler, the production cost is more reasonable and the method is more suitable for industrial production.

The invention relates to a synthetic route which takes o-fluoro-nitrolbenzene as starting raw material to prepare olanzapine, which comprises five steps: coupling, saponification, esterification, sulfur substitution and deoxidation.

The invention discloses a method for synthesizing poly-substituted 2-aryl benzothiazoles by utilizing thiourea as a sulphur source. According to the method, thiourea reacts with benzyl chloride to generate an S-benzylisothiourea salt in situ. After that, through the aromatic nucleophilic substitution reaction of the obtained S-benzylisothiourea salt with 2-fluoronitrobenzene and then the one-step reduction (one-pot reaction) process, o-amino phenyl benzyl thioether as an intermediate product can be obtained. Finally, through the iron-catalyzed cross-dehydrogenative-coupling reaction of the o-amino phenyl benzyl thioether, a target product can be obtained. Compared with the traditional synthetic method, the method has the significant advantages of (1) short reaction step, wherein the target product can be synthesized through only three steps of simple reactions by utilizing simple chemical raw materials; (2) mild reaction condition, high atom economy, and relatively safe and cheap reaction reagents; (3) high reaction yield, good substrate tolerance and free of any dangerous or high-toxicity reagent. Therefore, the method might be applied to the large-scale production.

The invention relates to a synthesis method of flurbiprofen. The synthesis method of the flurbiprofen belongs to the technical field of drug synthesis, and comprises the steps of adopting o-fluoronitrobenzene as a starting material; carrying out substitution reaction, coupled reaction and hydrolysis reaction in an organic solvent to obtain the target product flurbiprofen. According to the synthesis method of the flurbiprofen provided by the invention, the raw material source is wide, the used organic solvent has no need to be subjected to nonaqueous treatment, the reaction safety coefficient is high, the process operation is simple, three wastes are less, and the obtained flurbiprofen has high yield and high purity.

The invention belongs to a method for preparing pharmaceutical intermediate, and discloses a method for preparing 3-fluorine-4 morpholinyl phenylamine, comprising the steps: (1) reducing o-fluoro-nitrobenzene to obtain o-fluoroaniline; (2) adding the o-fluoroaniline and deacidifying agent into organic solvent, and slowly adding disubstituted ethyl ether into a reaction system at the temperature of100-150 DEG C and then stirring at the temperature of 100-200 DEG C to react for preparing o-fluoro-morpholinyl benzene; (3) taking nitric acid with the mass percent of 65-98% as nitrating agent andacetic acid as solvent, and leading the o-fluoro-morpholinyl benzene obtained in the step (2) to have nitration reaction to obtain 3-fluorine-4 morpholinyl nitrobenzene; (4) reducing the 3-fluorine-4morpholinyl nitrobenzene obtained in the step (3) and obtaining the 3-fluorine-4 morpholinyl phenylamine. As the method takes the o-fluoro-nitrobenzene as initial reactant, the price of the raw materials is low, and the production cost can be reduced. Meanwhile, no waste water containing fluorine is generated in the preparation process of the method, so that the method has little environmental pollution and is environment-friendly.

The invention relates to a one-pot synthesis method of an anticancer drug ceritinib intermediate 1-(isopropylsulfonyl)-2-nitrobenzene, which comprises the following steps: adding ortho-fluoronitrobenzene and sodium hydride into a solvent DMF (N,N-dimethylformamide), adding isopropyl mercaptan, reacting completely to obtain a 2-(isopropylthioether)nitrobenzene reaction solution, dropwisely adding acetic acid into the 2-(isopropylthioether)nitrobenzene reaction solution, carrying out oxydol oxidizing reaction, and after the reaction is complete, carrying out after-treatment to obtain the 1-(isopropylsulfonyl)-2-nitrobenzene. The potassium carbonate is changed into the strong alkali sodium hydride, thereby greatly lowering the reaction temperature and enhancing the reaction rate; after the synthetic reaction of the 2-(isopropylthioether)nitrobenzene, the next oxidizing step is directly performed without after-treatment, thereby avoiding the stink caused by after-treatment; and the method is applicable to industrial production, is convenient to operate, and is economical and environment-friendly.

The invention belongs to the technical field of medicine synthesis, and especially relates to a synthetic method of an anti-cancer drug ceritinib intermediate 1-amino-2-(isopropyl sulfonyl)benzene. The synthetic method comprises the following steps: employing o-fluoronitrobenzene, sodium hydride and isopropyl mercaptan to synthesize a 2-(isopropyl sulfide) nitrobenzene crude product, then directly reducing the crude product to iron powder, forming salt to obtain the 2-(isopropyl sulfide) aniline hydrochloride, and finally dropping hydrogen peroxide for oxidation in 2-(isopropyl sulfide) aniline hydrochloride for oxidation, forming salt, and dissociating to obtain a target product. The synthetic method has the advantages of simpleness, little sewage amount, low energy consumption, low production cost, and the product has the advantages of high purity, high yield, and easy industrial production, and is suitable for further popularization and application.

The invention discloses a preparation method of o-fluoroaniline, which relates to the field of organic synthesis, and specifically comprises the following steps: in a continuous reactor, the system is filled with water, and after three times of nitrogen replacement, the temperature is raised to 80°C, and the system is simultaneously pumped Put in o-fluoronitrobenzene, catalyst, inhibitory dehalogenation agent, water, (catalyst, inhibitory dehalogenation agent and water are mixed, stir evenly and pour in together) and hydrogen gas is introduced at the same time to ensure a pressure of 2.0MPa. Keep feeding continuously, the product is stratified through the stratified tank, and the product is obtained from the lower layer. Apply to the upper water layer. The preparation method disclosed by the invention is suitable for continuous large-scale production of o-fluoroaniline, has simple operation, high product purity and high yield, and the percentage content of the dehalogenated product is reduced to 0.02%.

The invention discloses a production process of o-fluoronitrobenzene. Fluorination is carryied out on main materials of o-chloronitrobenzene and potassium fluoride, and then after vacuum distillation and rectification, the o-fluoronitrobenzene product can be obtained. The process has scientific and reasonable design and adopts DMF as the solvent which is easy to be recycled and has high reaction efficiency; and simultaneously, tetramethylammonium chloride as the catalyst is cheap and has high reaction activity, thus saving the cost.

The invention discloses a method for synthesizing benzothiazole derivatives. Thiourea is used as a sulfur source, and the thiourea and o-fluoronitrobenzene derivatives are continuously converted into the benzothiazole derivatives by means of three-step conversion. The method includes enabling 2-benzylthio-benzamide derivatives to react to trifluoroacetic acid and the thiourea to obtain reaction products, extracting the reaction products by the aid of n-hexane, concentrating n-hexane layers to obtain the benzothiazole derivatives, and adding the o-fluoronitrobenzene derivatives and sodium hydroxide solution into lower-layer water phases to obtain 2-benzylthio-nitrobenzene derivatives; reducing tin dichloride to obtain 2-benzylthio-aminobenzene derivatives; ultimately acylating the 2-benzylthio-aminobenzene derivatives to obtain 2-benzylthio-substituted benzamide analogs. The method has the advantages of simplicity, environmental protection and low cost.