专利号:US-10730904-B2 优先权日:2012-11-14 标 题:Method for liquid-phase synthesis of nucleic acid 发明人:NONOGAWA MITSURU; NAGATA TOSHIAKI; SAITO HIDEKI; YASUMA TSUNEO 权利人:TAKEDA PHARMACEUTICALS CO 摘要:In this method, an oligonucleotide represented by formula (II) [wherein Y 1 , Q, Base, r and r′ are each as defined in claim 1 ] is prepared by using, as a synthesis unit, a novel nucleoside monomer compound represented by formula (I) [wherein X, R 1 , Y, Base, Z, Ar, R 2 , R 3 and n are each as defined in claim 1 ]. The novel nucleoside monomer compound is a nucleoside, the base moiety of which is substituted with an aromatic-hydrocarbon-ring-carbonyl or -thiocarbonyl group having at least one hydrophobic group. The method can dispense with column-chromatographic purification in every reaction, and enables base elongation not only in the 3′-direction but also in the 5′-direction, thus attaining efficient liquid-phase mass synthesis of an oligonucleotide.
专利号:WO-2025109557-A1 优先权日:2023-11-24 标题:Process for the synthesis of monoesters of ethylenediaminetetraacetic acid 发明人:TERAZONO YUICHI 权利人:NUTRIEN AG SOLUTIONS CANADA INC 摘要:A process for the synthesis of a compound of Formula (I) is provided. (I) wherein R is selected from the group consisting of alkyl, alkenyl, alkynyl, and steroidyl. The process comprises reacting a compound of Formula (IIa), Formula (IIb) or a mixture thereof with a compound of Formula R-X, to obtain a compound of Formula (IIIa), a compound of Formula (IIIb) or a mixture thereof, wherein A+ is a cesium cation, a quaternary ammonium cation or a quaternary phosphonium cation, and X is a leaving group; and reacting the compound of Formula (IIIa), compound of Formula (IIIb) or mixture thereof with an acid to obtain a reaction product which comprises the compound of Formula (I). (IIa) (IIb) (IIIa) (IIIb)
专利号:WO-2012150292-A1 优先权日:2011-05-03 标题:Stereoselective synthesis of cis-4-methylsphingosine and derivatives thereof 发明人:ARENZ CHRISTOPH; PROKSCH DENNY 权利人:UNIV BERLIN HUMBOLDT; ARENZ CHRISTOPH; PROKSCH DENNY 摘要:The invention provides for synthesis of a (S-R) dihydroxy-amino-methylalkylene characterized by the general formula I, or its R-S diastereomer, wherein R1 is CH2OH or CH2-CH2OH, and R2 is C2 to C20 alkyl, whereby a compound characterized by the general formula II, with R3, R4 and R5 being protecting groups for amino and hydroxyl functions, respectively, is used as a starting material. The invention further provides novel intermediates for syntheses of, and analogues to, cis-4-methylsphingosine.
专利号:US-3764626-A 优先权日:1969-12-23 标 题:Method of synthetizing tertiary aliphatic amines by amination of alkyl halides 发明人:PIVETTE P 权利人:PIERREFITTE AUBY SA 摘要:This invention is directed to the production, by synthesis, of tertiary aliphatic amines by amination of alkyl haloids, by means of secondary aliphatic amine, wherein a reaction mixture is prepared which consists of two fractions, one fraction comprising at least one alkyl haloid consisting mainly of halogen-1-alkane, the other fraction consisting of a secondary aliphatic amine within an aprotic dipolar solvent capable of dissolving the halide and the secondary amine but not of appreciably dissolving in the cold state the resulting tertiary aliphatic amine, whereby operation at relatively low temperatures and pressure values can be performed.
专利号:US-3728393-A 优先权日:1968-10-31 标题:Process of synthesis of long-chain aliphatic amines 发明人:GAIGE R; SCHNEIDER G 权利人:PROGIL 摘要:Process of synthesizing long-chain aliphatic primary amines by reacting 1-bromo-alkanes with an excess of ammonia at a temperature not exceeding the critical temperature of ammonia, for example at 60*-130*C, under a pressure of 5 to 40 atmospheres in the presence of a solvent which is a mixture of an organic compound and water which forms an homogeneous minimum boiling point azeotrope.
专利号:WO-2024112637-A1 优先权日:2022-11-21 标 题:Novel methods for chemical synthesis of glycosylated sphingosines 发明人:CHEN XI; YU HAI; GUCCHAIT ARIN; AGRAHARI ANAND KUMAR 权利人:UNIV CALIFORNIA 摘要:Described herein are novel methods of preparing sphingosines and glycosylated sphingosines. A method of preparing a glycosylated sphingosine as described herein includes an efficient, four-step route for synthesizing lactosylsphingosine (LacbβSph) from Garner's aldehyde. Also described herein is a cost-effective method of synthesizing a variety of glycosylated sphingosines, sphingosines and glycosyl acceptors, including both the d18:1 and d20:1 D-erythro-sphingosines and the d18:1 and d20:1 D-erythro-sphingosine glycosyl acceptors, from xylose.
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