1971results about How to "High synthesis efficiency" patented technology

The invention relates to the field of polypeptides, in particular to a method for preparing semaglutide. The method has the advantages that Fmoc-Lys (Alloc)-OH protection amino acid is used as a raw material, de-protection is carried out by the aid of selected Pd (PPh3) 4, accordingly, operation procedures are simple, only 1-2 times of simple elimination reaction operation are required, each elimination reaction operation is carried out for 10-30 min, side reaction is prevented, the operation procedures are safe, and enlarged production can be facilitated; Boc-His (Boc)-OH. DCHA and Boc-His (Trt)-OH are used as raw materials in the procedures, and accordingly His racemization risks can be reduced to the greatest extent; special fragments are coupled, and accordingly the synthesis efficiency can be improved.

The invention aims to provide a preparation method and application of a porous nano metal organic framework material, and is characterized in that the preparation method comprises the steps: adding a metal ion, an organic ligand, a surfactant and a nanocrystalline guide agent or a reagent forming the nanocrystalline guide agent into a growth medium, forming a framework structure through chemical complexation, crystallizing, filtering, washing, drying, and finally obtaining the porous nano metal organic framework material. The addition amount of the surfactant is 0-30% of the molar concentration of the metal ion; the metal ion is one or more of Cu<II>, Al<III>, Mg<II>, Fe<III>, Ni<II>, Co<II> and Zn<II>; the organic ligand has at least one atom independently selected from oxygen, sulfur and nitrogen and can be subjected to coordinated complexation to the metal ion through the atom. The method not only can effectively suppress the size of MOFs materials, but also easily improves size homogeneity and synthetic efficiency of the product.

The invention discloses a self-adaptation camouflage design method based on a background. According to the method, on the basis of a texture synthesis algorithm based on pixels, a whole camouflage image is synthesized pixel by pixel; in the synthesis process, a self coding algorithm is adopted to extract a texture primitive containing background sample complete texture features, and a neighborhood of the pixels to be synthesized is determined; by means of the neighboring correlation principle and a helix supplement search mechanism, a neighborhood matched with a target pixel neighborhood is searched for in a background sample; similarity matching is carried out through a pixel and texture similarity matching rule, pixels in the neighborhoods which are most similar in the sample are selected to serve as synthesis pixels, pixels of a target image are synthesized according to the sequence of scanning lines, and after synthesis, color quantization is carried out on the image by means of the clustering algorithm to generate a final camouflage image. By means of the method, similar camouflage images can be synthesized quickly according to the background, and the application aim of quickly camouflaging a target in a self-adaptation mode can be achieved.

The TS-1 molecular sieve preparing process features that surfactant is added into the mother liquid for synthesizing the molecular sieve, so that most of the silicon source and titanium source after hydrolysis agglomerate into solid grains. After the solid grains are filtered out and crystallized, the filtrate containing small amount of residual silicon source and titanium source is used as the alkali source for hydrolyzing the newly added silicon source and titanium source for synthesizing the next batch of molecular sieve. The process has greatly reduced environmental pollution, lowered preparation cost and raised synthesizing efficiency and benefit.

The invention provides an indoline compound of 1-(3-substituted benzoyl alkoxypropyl)-5-(2-nitrylpropyl)-7-cyanophoric indoline and a preparation method thereof. The indoline compound can be used as an intermediate compound and is used for synthesizing silodosin. The indoline compound uses substituted phenylformic acid as a raw material, is prepared by multiple-step reaction, has high yield and is easy to industrially produce.

The invention relates to a method for preparing Semaglutide through solid and liquid combination, and solves the technical problems that in the process for synthesizing long-sequence polypeptide by the existing technology, the synthesis period is long; the purification difficulty is high; the yield is low. The method for preparing Semaglutide through solid and liquid combination provided by the invention is characterized in that firstly, Lys and resin are condensed in an Alloc-Lys(Fmoc)-OH form by adopting a solid phase synthesis method; Fmoc protecting groups on epsilon-NH2 are removed; sidechain connection is performed; cracking is performed to obtain Alloc-Lys(PEG-PEG-gamma-Glu(OtBu)-Monobutyl octadecanate)-OH; meanwhile, 10 dipeptide or tripeptide or tetrapeptide fragments are simultaneously synthesized by a liquid phase synthesis method; then, the condensation reaction of the synthesized peptide fragments and single amino acid is performed by using the resin as a carrier; the 15-step solid phase condensation reaction is reduced in the process; the generation of lacked peptide impurities is reduced; the product purity and the yield are improved; meanwhile, the generation of the impurities of [+Gly]-Semaglutide and [+Ala]-Semaglutide is effectively avoided; the purification difficulty is greatly reduced. The method is widely applied to the technical field of polypeptide medicine preparation.

The invention provides a method for preparing a core-shell ferroferric oxide/graphene oxide composite nano-catalyst. The method comprises the following steps of preparing nanometer ferroferric oxide by utilization of a hydrothermal method, preparing graphene oxide by utilization of a modified Hummers method, preparing the core-shell ferroferric oxide/graphene oxide composite nano-catalyst by utilization of an electrostatic self-assembly method. The catalyst prepared according to the method provided by the invention has the advantages that the adsorptive property is excellent, the stability is good, the catalyst can be cyclically utilized, and an excellent adsorption effect can be achieved during the process of degrading simulated dye rhodamine B.

The invention provides poly(ethylene 2,5-furandicarboxylate), which contains the repeating units shown in formula (I) and has a characteristic viscosity not smaller than 0.2 dL/g. The invention also provides a preparation method for poly(ethylene 2,5-furandicarboxylate) provided by the technical scheme, which comprises the following steps of: carrying out esterification reaction on 2,5-furandicarboxylic acid and ethylene glycol under the action of a tin catalyst to obtain a first intermediate product, wherein the esterification reaction pressure is 0.1-0.4 MPa; and carrying out condensation polymerization reaction on the first intermediate product under the pressure of 10-70 Pa to obtain poly(ethylene 2,5-furandicarboxylate). Experiments show that poly(ethylene 2,5-furandicarboxylate) provided by the invention is dark brown, and has a characteristic viscosity of not smaller than 0.2 dL/g, a glass transition temperature of 60-63 DEG C and a melting point of 210-215 DEG C.

The invention relates to a cow rumen fermentation accelerator, which comprises bacterial broth and complex carbohydrate, wherein the weight ratio of the bacterial broth to the complex carbohydrate is 1:1-2, the bacterial broth comprises 1.0-2.0 * 1010CFU/ml beer yeast, 1.5-2.0 * 1010CFU/ml bacillus subtilis, 1.5-2.0 * 1010CFU/ml bacillus licheniformis, 1.0-2.0 * 109CFU/ml lactic acid bacteria, and 1.0-2.0 * 109CFU/ml aspergillus oryzae. The complex carbohydrate comprises 60-70 percent by weight of lactose, 15-25 percent by weight of fructose, 4-6 percent by weight of fumaric acid, 2-4 percentby weight of malic acid, 4-6 percent by weight of sodium bicarbonate and 1-3 percent by weight of magnesium oxide. Due to the cow rumen fermentation accelerator disclosed by the invention, the activity of cow rumen microorganism can be improved, the degradation of coarse fodder in rumen is promoted, the utilization ratio of nitrogen is improved, the output of MCP is increased, and thus the purpose of promoting the function of cow rumen fermentation is achieved.

The invention discloses a organic silicon compound containing silicon-silicon bond, silicon-carbon bond, silicon-halogen bond and ceramics precursor poly carbon silicon alky synthesized under high pressure and with medium in supercritical fluid status which uses mixture of the aforementioned compound as raw material, uses solvent soluble of poly carbon silicon alky as supercritical fluid medium. Ceramics precursor poly carbon silicon alky with different molecular weight and different softening point can be obtained by controlling reaction condition of synthesis. The inventive method effectively improves uniformity of heat transfer and reaction, with short reaction time, high synthesis efficiency, high synthesis yield. The produced poly carbon silicon has a high molecular weight, high content of bonds of silicon and hydrogen and uniform distribution of molecular weight. The inventive method can be widely used in preparation of SiC fibre, SiC composite, heat resistant alloy with high strength, ceramic binder, SiC membrane, nano-wire, nano-pipe and nano-powder and so on.

The invention provides an electric field activated sintering method of a solid electrolyte material Li7La3Zr2O12 (LLZO). The electric field activated sintering method comprises the following specific steps: ball-milling with a ball and mixing Li2O, La2O3 and ZrO2 powder, the mass percents of which are respectively 9.2-15.5%, 56.2-60.4% and 28.3-30.4%, wherein a zirconium oxide ball is used as a ball-milling medium, isopropanol is used as a solvent, and the ball-milling time is 12-36 hours; carrying out vacuum drying on ball-milling milled powder for 6-12 hours at the temperature of 80 DEG C; and carrying out electric field activated sintering, wherein the temperature is in the range from 800 to 1230 DEG C, the pressure is 0-100 MpaMPa, and a sintered sample has the room-temperature lithium-ion conductivity greater than 6*10<-4S>S/cm. Compared with a conventional solid-phase synthesis method, the electric field activated sintering method has the advantages that the synthesis reaction and the sintering compact process are completed in one step, the synthetic efficiency is improved to a large extent, the preparation technology is simplified, and the LLZO with the high lithium-ion conductivity is obtained.

The invention provides a synthesis process of carbetocin. The synthesis process comprises the following steps: performing a coupling reaction on Fmoc-Gly-OH with Rink Amide-AM Resin obtained in the first step to obtain Fmoc-Gly-Rink Amide-AM Resin; performing deprotection (20% piperidine) with DBLK to obtain H-Gly-Rink Amide-AM RFesin, and orderly completing the coupling of the H-Gly-Rink Amide-AM Resin with Fmoc-Leu-OH, Fmoc-Pro-OH, Fmoc-Cys(Trt)-OH, Fmoc-Asn(Trt)-OH, Fmoc-Gln(Trt)-OH, Fmoc-Ile-OH, Fmoc-Tyr(Me)-OH and tetrachlorobutyric acid until carbetocin linear peptide resin is synthesized; mixing a cracking agent with the carbetocin linear peptide resin obtained in the fourth step to have a cracking reaction, thereby removing the Rink Amide-AM Resin and side chain protecting groups; cyclizing the carbetocin linear crude peptide into a carbetocin crude product, and separating and purifying the carbetocin crude product to obtain the carbetocin. The synthesis process has the advantages that the polymerization side reaction is prevented, the process route is greatly simplified, the production cost is reduced and the synthesis efficiency is improved; in addition, the purity of the finished product is high; in short, the synthesis process is convenient for large-scale production, and meanwhile, advantageous for environmental protection, and has remarkable economic and social benefits.

The invention discloses a production method of 2-acrylamide-2-methylpropanesulfonic acid. The method comprises the steps of (1) mixing acrylonitrile with a sulfonating agent to form an acrylonitrile solution of the sulfonating agent; (2) enabling the acrylonitrile solution of the sulfonating agent, obtained in the step (1), to be in contact with isobutylene to form a pasty product; (3) filtering the pasty product to obtain a filter cake containing 2-acrylamide-2-methylpropanesulfonic acid; (4) washing the filter cake containing the 2-acrylamide-2-methylpropanesulfonic acid, obtained in the step (3), by using glacial acetic acid, thereby obtaining an AMPS crude product. By adopting the method, the synthesis time of the 2-acrylamide-2-methylpropanesulfonic acid can be effectively reduced, the synthesis efficiency is improved, and the cost is reduced. Moreover, the obtained product is high in yield and purity.

The invention provides an in vitro protein synthesis system, a kit and a preparation method. The in vitro protein synthesis system includes: (a) a cell extract; (b) an adsorbent used for enhancing protein synthesis efficiency; (c) amino acids; (d) nothing or NTPs; and (e) exogenous DNA molecules. A method for enhancing in vitro protein synthesis efficiency is provided. The method adopts the synthesis system and includes the following steps: (1) performing mixing; (2) adding the exogenous DNA molecules; (3) performing incubation synthesis; and (4) performing post-processing; and the method alsoincludes a step of adding the adsorbent after the step (1) or (2). In addition, the kit of the in vitro protein synthesis system is also provided. Therefore, the synthesis efficiency of foreign protein can be significantly enhanced.