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34results about How to "Reasonable synthetic route" patented technology

Cigarette aroma enhancement humectant 1-L-leucine-1-deoxidation-D-fructose and preparation method thereof

The invention discloses cigarette aroma enhancement humectant 1-L-leucine-1-deoxidation-D-fructose. The structural formula of the cigarette aroma enhancement humectant 1-L-leucine-1-deoxidation-D-fructose is as follows. The invention further discloses a preparation method of the compound. D-mannose is taken as a raw material, and the cigarette aroma enhancement humectant 1-L-leucine-1-deoxidation-D-fructose is successfully synthesized through simple reaction processing. Physical humectant performance tests and inherent sensory quality evaluations show that the humectant has a good physical humectant effect on cigarettes, and can reduce irritation and blended gases of the cigarettes and improve the smoke mellow sense and comfort of the cigarettes.
Owner:CHINA TOBACCO HENAN IND +1

Degradable aqueous polyurethane dispersion and preparation method thereof

The invention relates to degradable aqueous polyurethane dispersion and a preparation method thereof. The dispersion comprises the following components in part by weight: 10 to 30 parts of polyol, 15 to 25 parts of diisocyanate, 3 to 8 parts of hydrophilic chain-extender, 1 to 3 parts of collagen, 3 to 5 parts of neutralizer, 45 to 55 parts of acetone, and 140 to 180 parts of deionized water. Themethod comprises the following steps: dehydrating the polyol under reduced pressure; adding the diisocyanate, the hydrophilic chain-extender, the collagen and the acetone into the polyol; reacting the mixture until the isocyano amount reaches a theoretical value; adding the neutralizer and the deionized water into the solution after the solution is cooled; and distilling the product to obtain thedegradable aqueous polyurethane dispersion. Compared with the prior art, the degradable aqueous polyurethane dispersion has the advantages of reasonable synthesis route, simple operation, high product stability, high water resistance, good degradability and sanitary performance, and can be used for package paint of foods, medicaments, cigarettes and other products.
Owner:SHANGHAI WEIKAI CHEM

Polymerisable fluorescent functional monomer and its prepn and use

The present invention relates to polymerisable fluorescent functional monomers in the structure as shown, and they have strong fluorescent reaction and part capable of reacting with biomacromolecular protein and non-covalent bond of DNA mutually. They may be polymerized with hydrophilic monomer to obtain fluorescent amphiphilic polymer with excellent biocompatibility, medicine carrying capacity and target administration capacity, and the polymer may find wide application foreground in high sensitivity fluorescent tracing detection technology, biomacromolecule separation and distinction, biosensor, medical diagnosis, medicine conveying, target material and other aspects. The present invention has reasonable synthesis path, simple synthesis process, easy-to-obtain material and high application value.
Owner:WUHAN UNIV

Bis-silicon-bridged dinuclear metallocene compound and preparation and application thereof

The invention relates to a bis-silicon-bridged dinuclear metallocene compound and preparation and application thereof. The bridged cyclopentadienyl rings of the bis-silicon-bridged dinuclear metallocene compound contain different substituents. Dimethyldichlorosilane reacts with cyclopentadienyl sodium, so that light yellow solution is obtained; the light yellow solution reacts with n-butyl lithium, and dimethyldichlorosilane is then added for reaction, so that bis-silicon-bridged dicyclopentadiene is obtained; the bis-silicon-bridged dicyclopentadiene reacts with n-butyl lithium, halogenide is then added for reaction, n-butyl lithium is then added for reaction, and finally, another halogenide is added for reaction, so that ligand L is obtained; and cyclopentadienyl titanium trichloride or cyclopentadienyl zirconium trichloride or substituetd cyclopentadienyl titanium trichloride or substituetd cyclopentadienyl zirconium trichloride is added in the ligand L, so that the compound is obtained. The synthesis route is reasonable, the yield is high, separation and purification are easy, the amount of needed cocatalysts is less when the compound is used for catalyzing the copolymerization of ethylene, such as ethylene / hexene-1, ethylene / octene-1 and ethylene / decylene, and long-chain Alpha-alkene, the catalytic activity is high, the insertion rate of the long-chain Alpha-alkene is high, and molecular weight distribution is wide.
Owner:PETROCHINA CO LTD +1

Novel tobacco humectant 3-O-hydroxyethyl-D-glucose and preparation method thereof

The invention discloses a novel tobacco humectant 3-O-hydroxyethyl-D-glucose. The structural formula is represented in the invention. The invention also discloses a preparation method of the novel tobacco humectant 3-O-hydroxyethyl-D-glucose. The novel tobacco humectant 3-O-hydroxyethyl-D-glucose is synthesized by taking D-glucose as a raw material, and introducing isopropylidene for protection and deprotection of the hydroxy of D-glucose. It is shown by physical humidity retention test and inner sensory quality evaluation that the humectant possesses excellent physical humidity retention performance on tobaccos, and is capable of reducing tobacco irritation and impure flavor, and increasing mellow flavor and comfortableness of the smoke of tobaccos.
Owner:CHINA TOBACCO HENAN IND +1

2-substituent-5-substitued anilino-1,3,4-oxadiazole derivative and synthesis method and application thereof

ActiveCN103980223ALow costExcellent anti-plant virus activityBiocideOrganic chemistryTobacco mosaic virusAniline
The invention discloses a compound 2-substituent-5-substitued anilino-1,3,4-oxadiazole derivative with functions of resisting plant germs and plant viruses and a preparation method and an application thereof, wherein the structure of the compound is represented by the general formula (I). In the invention, the substituted arylamine is adopted as a start raw material, and a thioether compound is prepared by the steps of esterification, hydrazinolysis, salifying, ring closing and etherification; a sulfone compound is prepared by thioether oxidization. The compound disclosed by the invention has a good inhibiting effect on gibberella zeae, pepper fusarium wilt pathogen, valsa mali and tobacco mosaic virus and can be used for preparing medicines resisting plant germs and plant viruses.
Owner:GUIZHOU UNIV

Preparation method for (2R,3S)-1-chlorine-3-tert-butoxycarbonylamino-4-phenyl-2-butanol

The invention provides a preparation method for (2R,3S)-1-chlorine-3-tert-butoxycarbonylamino-4-phenyl-2-butanol. The preparation method comprises the steps that L-phenylalanine is taken as raw materials, protected by adopting benzyl, esterified and then catalyzed through NMM to generate a mixed anhydride compound, the mixed anhydride compound reacts with diazomethane to generate diazoketone, a reduction reaction and palladium carbon reduction are performed, and finally the intermediate (2R,3S)-1-chlorine-3-tert-butoxycarbonylamino-4-phenyl-2-butanol is obtained. According to the preparation method, the low-cost benzyl is adopted to protect amidogen, the synthetic route is reasonable, the operation technology is simple, safe and high in yield, industrialization can be well achieved, and the production efficiency is improved.
Owner:SHANGHAI APPLIED TECHNOLOGIES COLLEGE

Preparation method of aripiprazole photodegradation impurities

The invention relates to a preparation method of aripiprazole photodegradation impurities, and belongs to the technical field of drug synthesis. According to the preparation method, 2,3-dichlorobenzenamine is taken as a raw material, a compound II is obtained via reaction of 2,3-dichlorobenzenamine with a compound V, and a target product compound I is obtained via reaction of the compound II with a compound III; wherein A in the compound V is used for representing Cl, Br, COOH, CHO, or COCl, A' is used for representing NH2 or NO2, and n is used for representing 1 or 2. The synthesis route of the preparation method is reasonable; the raw materials are easily available; operation is convenient and simple; yield of the target product is high; and purity is high.
Owner:REYOUNG PHARMA

Method for preparing Anilofos by recycled ammonium thiophosphate salt from phosphorus-containing wastewater

The invention discloses a method for preparing Anilofos by recycled ammonium thiophosphate salt from phosphorus-containing wastewater, the method comprises the following operation steps: (1) after themalathion synthesis reaction is finished, quantitative pure water is added into malathion process oil, ammonia water is slowly dripped, and the mixture is left standing for layering to obtain methylsulfide ammonium salt solution; (2) adding p-chloronitrobenzene, acetone, catalyst and solvent methanol into a high-pressure reaction kettle in sequence, and introducing hydrogen to enable the internal pressure to reach 0.20-0.35 MPa; and (3) N-isopropyl p-chloroaniline and chloroacetyl chloride are reacted to generate an intermediate N-isopropyl-N-chloroacetyl p-chloroaniline, and finally N-isopropyl-N-chloroacetyl p-chloroaniline is subjected to solid reaction with methyl sulfide ammonium salt to finally prepare the Anilofos. The method for preparing the Anilofos by the recycled ammonium thiophosphate salt from the phosphorus-containing wastewater is simple to operate, and is green and environment-friendly, and the prepared intermediate of the ammonium thiophosphate salt can be completely used for synthesizing the Anilofos without affecting the quality of the final product.
Owner:潍坊新绿化工有限公司

Method for synthesizing pyrazole compound based on WK (Willgerodt-Kindler) reaction and VHA (Vilsmeier-Haack-Arnold) reaction

The invention discloses a method for synthesizing a pyrazole compound based on WK (Willgerodt-Kindler) reaction and VHA (Vilsmeier-Haack-Arnold) reaction. The method comprises the steps that an acyl compound is taken as a raw material to synthesize a carboxylic compound through the WK reaction; a VHA reagent is prepared; the carboxylic compound is added into the VHA reagent to synthesize an oniumsalt condensing agent; the onium salt condensing agent is hydrolyzed to obtain an aldehyde compound; the aldehyde compound is reacted with hydrazine hydrate to obtain the pyrazole compound. The methodhas the advantages that the synthetic route is reasonable, the method is stable and reliable, the synthetic efficiency is high, and the carboxylic compound, the onium salt condensing agent, the aldehyde compound and the pyrazole compound can be obtained simultaneously; the method has wide application prospect and huge commercial value, enriches the variety of inorganic and organic compounds as well as the synthetic method in the inorganic and organic field.
Owner:CHINA UNIV OF GEOSCIENCES (WUHAN)

Tedizolid impurity and preparing method thereof

The invention relates to a tedizolid impurity and a preparing method thereof, and belongs to the technical field of drug synthesis. The tedizolid impurity exists in the following tedizolid steps, and please see the steps in the specification, wherein X is fluorine, chlorine, bromine, iodine, tosylate or methanesulfonate, and R is organic boronic acid organic borate ester; and please see the structural formula of the impurity in the specification. The tedizolid impurity is of great significance in deep surveying of the tedizolid. The invention further provides a preparing method which is simple in process.
Owner:REYOUNG PHARMA

Novel tobacco humectant 3-O-carboxymethyl-D-glucose and preparation method thereof

The invention discloses a novel tobacco humectant 3-O carboxymethyl-D-glucose. The fork group protects and deprotects the hydroxyl group of D-glucose, and successfully synthesizes the new polyhydroxy tobacco humectant—3-O-carboxymethyl-D-glucose. Through the physical moisturizing performance test and the internal sensory quality evaluation, it was found that the humectant has a good physical moisturizing effect on cigarettes, and can reduce the irritation and miscellaneous gas of cigarettes, and improve the roundness and comfort of cigarette smoke.
Owner:CHINA TOBACCO HENAN IND +1

Novel humectant 3-o-hydroxyethyl-d-glucose for cigarettes and preparation method thereof

The invention discloses a novel tobacco moisturizer 3-O-hydroxyethyl-D-glucose. The propylidene group protects and deprotects the hydroxyl group of D-glucose, and successfully synthesizes the novel polyhydroxy cigarette humectant 3-O-hydroxyethyl-D-glucose. Through the physical moisturizing performance test and the internal sensory quality evaluation, it was found that the humectant has a good physical moisturizing effect on cigarettes, and can reduce the irritation and miscellaneous gas of cigarettes, and improve the roundness and comfort of cigarette smoke.
Owner:CHINA TOBACCO HENAN IND +1

Constrained geometry carbon-bridged single metallocene compound, its preparation and application

The invention relates to a constrained geometry carbon-bridged single metallocene compound, its preparation and application; a structural general formula is shown as the following: wherein R denotes H, or allyl or t-butyl containing 1 to 10 carbon atoms; R1,R2 denote H, Or alkyl, allyl, aromatic base or silicon-based containing 1 to 10 carbon atoms; M denotes Ti or Zr; Cp denotes cyclopentadienyl, substituted cyclopentadienyl, indenes or substituted indenes. The application of the constrained geometry carbon-bridged single metallocene compound is suitable for catalyzing ethane / 1- hexane, ethane / 1-octene copolymerization, reaction temperature is 70 DEG C, the reaction time is 0.5 hour, the aluminum / zirconium ratio is 1000, the concentration of 1-octene is 0.6 mol / L and ethene pressure is 0.1 MPa, polymerization activity is 2.76*106 g PE / mol.cat.h., the 1-octene content in polymer is 19.07%, catalytic activity is high during copolymerization, the insertion rate of the long chain alpha-alkene is high.
Owner:PETROCHINA CO LTD +1

Polymerisable fluorescent functional monomer and its prepn and use

The present invention relates to polymerisable fluorescent functional monomers in the structure as shown, and they have strong fluorescent reaction and part capable of reacting with biomacromolecular protein and non-covalent bond of DNA mutually. They may be polymerized with hydrophilic monomer to obtain fluorescent amphiphilic polymer with excellent biocompatibility, medicine carrying capacity and target administration capacity, and the polymer may find wide application foreground in high sensitivity fluorescent tracing detection technology, biomacromolecule separation and distinction, biosensor, medical diagnosis, medicine conveying, target material and other aspects. The present invention has reasonable synthesis path, simple synthesis process, easy-to-obtain material and high application value.
Owner:WUHAN UNIV

A kind of preparation method of tedizolid impurity

The invention relates to a preparation method of tedizolid impurity, which comprises the steps of treating compound A with a strong base in the presence of oxygen, adding glycidyl ester, and reacting to obtain tedizolid impurity. The high-purity tedizolid impurity can be prepared by the method, and the method has high yield and simple operation, and the product can be used as a reference substance of the tedizolid impurity, and then the purity of the intermediate is monitored in the synthesis process of the tedizolid.
Owner:BEIJING WINSUNNY PHARMA CO LTD

Preparation method of HIF-2alpha inhibitor PT2385

The invention relates to a preparation method of an HIF-2 alpha inhibitor PT2385. The method comprises the following steps of: performing Friedel-Crafts reaction on p-difluorobenzene serving as a raw material and 3-chloropropionyl chloride to generate an intermediate II, performing substitution reaction on the intermediate II and sodium methyl mercaptide to generate an intermediate III, performing oxidation, reduction and two-step substitution reaction to obtain an intermediate VII, performing oxidation reaction on the intermediate to obtain an intermediate VIII, and reacting the intermediate VIII with n-butylamine to obtain a compound IX, carrying out fluorination reaction and hydrolysis to obtain an intermediate X, and finally carrying out asymmetric reduction reaction to obtain a final product PT2385. Compared with the existing synthesis method, the process route provided by the invention has the obvious advantages that the raw materials are cheap and easy to obtain, the operation is simple and convenient, the number of reaction steps is small, the total yield is up to 47.6%, multi-step high-temperature reaction is avoided, and industrial production is easy.
Owner:CHINA PHARM UNIV

Preparation method and application of amino acid ester compound containing 4-piperidyl-6-methylpyrimidine heterocyclic ring

The invention discloses a preparation method and bioactivity of an amino acid ester compound containing a 4-piperidyl-6-methylpyrimidine heterocyclic ring, which is used for preventing and controllingcucumber mosaic virus, and relates to a compound shown as a general formula (I) and a preparation method thereof. The invention provides the amino acid ester compound containing the 4-piperidyl-6-methylpyrimidine heterocyclic ring, which is synthesized by taking 2-amino-4-piperidyl-6-methylpyrimidine, substituted aldehyde and malonate as raw materials and p-xylene as a solvent through a microwaveone-pot method. The compound I2 provided by the invention has a relatively good inhibition effect on the cucumber mosaic virus and tobacco ralstonia solanacearum. The formula I is shown in the description.
Owner:GUIZHOU INST OF TECH

Method of synthesizing onium salt type condensation agent on the basis of WK reaction and VHA reaction

The invention discloses a method of synthesizing an onium salt type condensation agent on the basis on the basis of a Willgerodt-Kindler reaction and a Vilsmeier-Haack-Arnold reaction. The method includes the steps of synthesizing a carboxylic acid compound through the Willgerodt-Kindler reaction with an acyl compound as a raw material; preparing a Vilsmeier-Haack-Arnold reagent; adding the carboxylic acid compound to the Vilsmeier-Haack-Arnold reagent to synthesize the onium salt type condensation agent. The method has reasonable synthesis route and stable and reliable process, is high in synthesis efficiency, can be used for producing the carboxylic acid compound and the onium salt type condensation agent at the same time, has great application prospect and huge commercial value and enriches types of inorganic and organic compounds and synthesis methods in inorganic and organic fields.
Owner:CHINA UNIV OF GEOSCIENCES (WUHAN)

Preparation method of 5,6-dihydro-3-(4-morpholinyl)-1-[4-(2-oxo-1-piperidinyl)phenyl]-2(1h)-pyridone

The invention provides a preparation method of 5,6-dihydro-3-(4-morpholinyl)-1-[4-(2-oxy-1-piperidyl) phenyl]-2(1H)-pyridine. The preparation method comprises the following steps: step (1) reducing N-(4-nitrobenzophenone)-3,3-dichloro-2-oxy piperidine (10) which is used as an initial raw material by utilizing a reducing agent to obtain a compound 13; step (2) acylating the compound 13 and 5-bromine valeryl chloride in the presence of catalyst and acid-binding agent to obtain a compound 14; step (3) facilitating the reaction of the compound 14 in the presence of cyclic condensation agent to obtain a compound 15; step (4) facilitating the reaction of the compound 15 and morpholine in the presence of alkali to obtain a compound 5, wherein the reaction route is as follows. Compared with the prior art, the preparation method has the advantages that the limitation of enamine structure on the synthesized pyridone ring can be avoided, the synthesis of the pyridone ring can be simplified, and the synthesizing route is more reasonable; fewer reaction side products are produced, easiness in purification is realized, the total yield is high, and simplicity in reaction operation is realized; the preparation method is very suitable for the industrialized production.
Owner:SHANGHAI SHYNDEC PHARMA CO LTD

A branched viscoelastic powder oil displacement agent and its preparation method

The present invention provides a branched viscoelastic powder oil displacement agent and its preparation method. The method is carried out as follows: a. Acrylamide aqueous solution is prepared according to the ratio of acrylamide: water = 100:200-250 parts by weight; b. First take the acrylamide aqueous solution in step a and put it into a three-neck container, and in a water bath at 10°C to 15°C, blow nitrogen gas for 15 to 30 minutes. The persulfide aqueous solution prepared according to the ratio and the polyhydroxy compound aqueous solution prepared according to the ratio of polyol: water = 0.0018 to 0.004: 40 to 60 parts by weight are added to a three-neck container for reaction, and after the temperature of the reaction solution exceeds 1 °C , stop the nitrogen flow, and start to record the temperature of the reaction system; c. When the temperature of the reaction system no longer rises, put the three-neck container in a water bath at 70-85°C and keep it warm for 4-6 hours, then take out the gel, dry it, Pulverize to obtain viscoelastic powder oil displacement agent products.
Owner:CHINA PETROLEUM & CHEM CORP +1

Synthesis method of 4-fluoro-5-isopropyl-2-methoxyphenylboronic acid

The invention discloses a synthesis method of 4-fluoro-5-isopropyl-2-methoxyphenylboronic acid. The method includes: starting from m-fluoroanisole, carrying out reaction with iodine to conduct iodination, then performing catalytic coupling with isopropylboronic acid, finally conducting selective deprotonation / boronation under a large steric hindrance alkali condition, and performing hydrolysis to obtain a product. The method has the advantages of reasonable route design, simple operation and high selectivity, and is suitable for industrial amplification.
Owner:CANGZHOU PURUI DONGFANG SCI & TECH

A flavoring and moisturizing agent 1-l-tryptophan-1-deoxy-d-fructose for tobacco and its preparation method

The invention discloses a flavor-enhancing moisturizer 1-L-tryptophan-1-deoxy-D-fructose for cigarettes. As a raw material, a flavor-enhancing humectant 1-L-tryptophan-1-deoxy-D-fructose for cigarettes was successfully synthesized through a simple reaction process. Through physical moisturizing performance tests and intrinsic sensory quality evaluations, it was found that The humectant has a good physical moisturizing effect on cigarettes, and can reduce the irritation and miscellaneous gas of cigarettes, and improve the roundness and comfort of cigarette smoke.
Owner:CHINA TOBACCO HENAN IND +1

A kind of preparation method of (2r,3s)-1-chloro-3-tert-butoxyamido-4-phenyl-2-butanol

The invention provides a preparation method for (2R,3S)-1-chlorine-3-tert-butoxycarbonylamino-4-phenyl-2-butanol. The preparation method comprises the steps that L-phenylalanine is taken as raw materials, protected by adopting benzyl, esterified and then catalyzed through NMM to generate a mixed anhydride compound, the mixed anhydride compound reacts with diazomethane to generate diazoketone, a reduction reaction and palladium carbon reduction are performed, and finally the intermediate (2R,3S)-1-chlorine-3-tert-butoxycarbonylamino-4-phenyl-2-butanol is obtained. According to the preparation method, the low-cost benzyl is adopted to protect amidogen, the synthetic route is reasonable, the operation technology is simple, safe and high in yield, industrialization can be well achieved, and the production efficiency is improved.
Owner:SHANGHAI INST OF TECH

Preparation of an amino acid ester compound and its use in preventing and treating tobacco diseases

The invention discloses a preparation method and biological activity of an amino acid ester compound containing a 4-(dimethoxymethyl)pyrimidine heterocycle, which is a compound for preventing and treating tobacco mosaic virus. It is composed of the following general formula ( I) the compound represented by it and the preparation method thereof. The present invention introduces the use of 4-(dimethoxymethyl)pyrimidin-2-amine, substituted aldehyde, and malonate as raw materials, toluene as solvent, and under ultrasonic conditions, a one-pot synthesis method containing 4-(dimethoxy) Amino acid esters of pyrimidine heterocycles. Compound I of the present invention 5 and I 8 It has good inhibitory effect on tobacco mosaic virus and tobacco bacterial wilt. (I).
Owner:GUIZHOU INST OF TECH

Bis-silicon-bridged dinuclear metallocene compound and preparation and application thereof

The invention relates to a bis-silicon-bridged dinuclear metallocene compound and preparation and application thereof. The bridged cyclopentadienyl rings of the bis-silicon-bridged dinuclear metallocene compound contain different substituents. Dimethyldichlorosilane reacts with cyclopentadienyl sodium, so that light yellow solution is obtained; the light yellow solution reacts with n-butyl lithium, and dimethyldichlorosilane is then added for reaction, so that bis-silicon-bridged dicyclopentadiene is obtained; the bis-silicon-bridged dicyclopentadiene reacts with n-butyl lithium, halogenide is then added for reaction, n-butyl lithium is then added for reaction, and finally, another halogenide is added for reaction, so that ligand L is obtained; and cyclopentadienyl titanium trichloride orcyclopentadienyl zirconium trichloride or substituetd cyclopentadienyl titanium trichloride or substituetd cyclopentadienyl zirconium trichloride is added in the ligand L, so that the compound is obtained. The synthesis route is reasonable, the yield is high, separation and purification are easy, the amount of needed cocatalysts is less when the compound is used for catalyzing the copolymerization of ethylene, such as ethylene / hexene-1, ethylene / octene-1 and ethylene / decylene, and long-chain Alpha-alkene, the catalytic activity is high, the insertion rate of the long-chain Alpha-alkene is high, and molecular weight distribution is wide.
Owner:PETROCHINA CO LTD +1

2-substituent-5-substituted anilino-1,3,4-oxadiazole derivatives and their synthesis method and application

ActiveCN103980223BLow costExcellent anti-plant virus activityBiocideOrganic chemistryPlant virusTobacco mosaic virus
The invention discloses a compound 2-substituent-5-substitued anilino-1,3,4-oxadiazole derivative with functions of resisting plant germs and plant viruses and a preparation method and an application thereof, wherein the structure of the compound is represented by the general formula (I). In the invention, the substituted arylamine is adopted as a start raw material, and a thioether compound is prepared by the steps of esterification, hydrazinolysis, salifying, ring closing and etherification; a sulfone compound is prepared by thioether oxidization. The compound disclosed by the invention has a good inhibiting effect on gibberella zeae, pepper fusarium wilt pathogen, valsa mali and tobacco mosaic virus and can be used for preparing medicines resisting plant germs and plant viruses.
Owner:GUIZHOU UNIV

A kind of preparation technology of amd3465

The invention discloses a novel preparation technology of molecule AMD3465 for treating hematopoietic stem cell symptoms. The chemical name of the molecule AMD3465 is 2-pyridine methylamino, N-((3-(1,4,8,11-tetraazacyclotetradecane-methyl)benzyl)methyl-). The novel preparation technology comprises the steps of: with 2-(aminomethyl)pyridine as a raw material, singly butting the 2-(aminomethyl)pyridine with p-Xylylene dibromide, then butting with tricarbonyl torus, and reducing to obtain the product AMD3465 (I), wherein the purity of the product AMD3465 (I) is above 99.5 percent. The novel preparation technology is reasonable in process route and simple and convenient to operation and has broad prospects of popularization and application.
Owner:SHANDONG LUBEI PHARMA
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