CAS: 1631-25-0; N-Cyclohexylmaleimide

上下游产品

CAS号108-31-6 顺酐 | CAS号108-91-8 环己胺 | CAS号31930-36-6 顺-3-碘丙烯酸乙酯 | CAS号3173-53-3 环己基异氰酸酯 | CAS号24564-83-8 2-Butenoic acid... | CAS号21477-59-8 (Z)-4-(环己基氨基)-4... | CAS号1314-23-4 氧化锆 | CAS号109-73-9 正丁胺 | CAS号541-59-3 马来酰亚胺 | CAS号108-93-0 环己醇 | CAS号62448-61-7 1-cyclohexyl-3,... | CAS号6301-71-9 N-(环庚基)丁二酰胺

(Z)-4-(环己基氨基)-4-氧亚基丁-2-烯酸置于sodium Acetate,乙酸酐体系中,化学反应 8.0H,反应生成N-环己基马来酰亚胺
参考文献:N-取代的酰亚胺的合成和抗菌活性.
标题:N-取代的酰亚胺的合成和抗菌活性.
摘要:在我们关于新型抗菌剂的研究计划领域中,合成了一系列n-取代的酰亚胺.这些化合物是通过将酰胺基酸在乙酸酐/乙酸钠或六甲基二硅氮烷/溴化锌中的羟基芳族衍生物环化而获得的.羟基烷基马来酰亚胺是通过将相应的氨基醇与马来酸酐在沸腾的甲苯中缩合而直接制备的.大多数n-取代的马来酰亚胺对来自atcc集合的细菌(金黄色葡萄球菌atcc 25923,粪肠球菌atcc 29212,大肠杆菌atcc 25922和铜绿假单胞菌atcc 27853)显示出有趣的抗菌活性,但铜绿假单胞菌的mic值始终很高( 128微克/毫升).具有烷基取代基的酰亚胺显示出比mic值在8-32 Microg / Ml范围内的芳族类似物更高的活性.相比之下,琥珀酰亚胺几乎没有活性.
Doi:10.1016/s0014-827X(02)01217-X

专利信息

专利号:US-5877278-A
优先权日:1992-09-24
标题:Synthesis of N-substituted oligomers
发明人：ZUCKERMANN RONALD N; GOFF DANE A; NG SIMON; SPEAR KERRY; SCOTT BARBARA O; SIGMUND AARON C; GOLDSMITH RICHARD A; MARLOWE CHARLES K; PEI YAZHONG; RICHTER LUTZ; SIMON REYNA
权利人:CHIRON CORP
摘要:A solid-phase method for the synthesis of N-substituted oligomers, such as poly (N-substituted glycines) (referred to herein as poly NSGs) is used to obtain oligomers, such as poly NSGs of potential therapeutic interest which poly NSGs can have a wide variety of side-chain substituents. Each N-substituted glycine monomer is assembled from two 'sub-monomers' directly on the solid support. Each cycle of monomer addition consists of two steps: (1) acylation of a secondary amine bound to the support with an acylating agent comprising a leaving group capable of nucleophilic displacement by -NH2, such as a haloacetic acid, and (2) introduction of the side-chain by nucleophilic displacement of the leaving group, such as halogen (as a solid support-bound alpha -haloacetamide) with a sufficient amount of a second sub-monomer comprising an -NH2 group, such as a primary amine, alkoxyamine, semicarbazide, acyl hydrazide, carbazate or the like. Repetition of the two step cycle of acylation and displacement gives the desired oligomers. The efficient synthesis of a wide variety of oligomeric NSGs using automated synthesis technology of the present method makes these oligomers attractive candidates for the generation and rapid screening of diverse peptidomimetic libraries. The oligomers of the invention, such as N-substituted glycines (i.e. poly NSGs) disclosed here provide a new class of peptide-like compounds not found in nature, but which are synthetically accessible and have been shown to possess significant biological activity and proteolytic stability. Combinatorial libraries of cyclic compounds are disclosed wherein the cyclic compounds are comprised of at least one ring structure derived from cyclization of a peptoid backbone. The diversity of product compounds is generated by the sequential addition of substituted submonomers. The combinatorial library includes 10 or more, preferably 100 or more, and more preferably 1,000 or more distinct and different compounds. The library includes each of the product compounds in retrievable and analyzable amounts and preferably includes at least one biologically active compound. Methods of synthesizing the combinatorial libraries and assay devices produced using the libraries are disclosed as is methodology for screening for and obtaining biologically active cyclic organic compounds.

专利号:US-5510516-A
优先权日:1990-07-06
标 题 :Process for selective epoxidation of unsaturated (meth)acrylates, new functional (meth)acrylates obtained and their application to the synthesis of new polymers
发明人：CAUBERE PAUL; FORT YVES; ORTAR AGNES
权利人:ATOCHEM
摘要:An unsaturated (meth) acrylic compound of formula: (I) (X=O, S, NH, NR3 (R3=C1-12-alkyl) or O-(CH2)n (where n=1-16 approximately); R2=C2-20 straight-chain or branched alkyl, monocyclic or polycyclic cycloalkyl or heterocycloalkyl, or alkylaryl hydrocarbon chain, comprising an olefinic double bond in the chain, or at the end of the chain in the case of alkyl or alkylaryl, or an exocyclic or endocyclic olefinic double bond in the case of monocyclic or polycyclic cycloalkyl or heterocycloalkyl; and R1=H or C1-5-alkyl), is reacted at 10 DEG -60 DEG C. with at least one oxidising compound (hydrogen peroxide) in the presence of at least one catalyst (alkali metal molybdates and tungstates) and in the presence of at least one phase transfer agent and when R2=polycyclic cycloalkyl or hetercycloalkyl, an organic peracid or hydrogen peroxide in the presence of at least one heteropolyacid. To open the epoxide function, the epoxide obtained is reacted with a compound chosen from strong inorganic acids, boron trifluoride etherate complexes, acid salts in the presence of the corresponding acid, halides of trialkylsilanes or trialkoxysilanes, and ketones in the presence of cationic resins.

专利号:US-7351781-B2
优先权日:2001-04-24
标题 :Synthesis of vinyl polymers by controlled radical polymerization
发明人：WHITE DANIELA; O'DWYER JAMES B
权利人:PPG IND OHIO INC
摘要:A controlled free radical polymerization process, which includes the steps of: adding a monofunctional iniferter compound to an oxygen-free solvent; heating the solution to a temperature sufficient to allow the iniferter compound to form two carbon centered radical residues; adding a first monomer composition comprising one or more monomers to the solution containing the radical containing residues; polymerizing the first monomer composition to form a quasi-living polymer; and optionally polymerizing a second monomer composition comprising one or more monomers, which are different than the first monomer composition. The resulting non-random copolymer having the general formula:n nφ-[-A p -B s -] t -φn nwhere A and B are different compositions of ethylenically unsaturated monomers; p is an integer from 1 to 1,000; s is an integer from 0 to 1,000; t is an integer from 1 to 100; and φ is a residue from the iniferter.

专利号:EP-0627420-B1
优先权日:1992-01-30
标 题 :Process for the synthesis of maleimide compound improved in storage stability
发明人：KITA YUICHI; NAKAGAWA KOICHI; KISHINO KAZUO
权利人:NIPPON CATALYTIC CHEM IND
摘要:A stabilized maleimide compound which is hardly discolored during storage, wherein the content of primary amines is 500 ppm or less, that of maleic anhydride is 5-2,000 ppm, and that of 2-amino-N-substituted succinimide is 300 ppm or less. It is preferable that the content of chlorine compounds be 10 ppm or less in terms of chlorine and that of volatile components having each a boiling point of 200 °C or below under an ordinary pressure be 2,000 ppm or less.

专利号:US-9012648-B2
优先权日:2012-08-21
标题 :Haptens of risperidone and paliperidone
发明人：HASPESLAGH PIETER RIK; VLIEGEN MAARTEN; HRYHORENKO ERIC; DECORY THOMAS R; SANKARAN BANUMATHI
权利人:JANSSEN PHARMACEUTICA NV; ORTHO CLINICAL DIAGNOSTICS INC
摘要:The invention relates to compounds of Formula I, wherein R1 and R2 are defined in the specification, useful for the synthesis of novel conjugates and immunogens derived from risperidone and paliperidone. The invention also relates to conjugates of a risperidone or paliperidone hapten and a protein.

专利号:US-9303041-B2
优先权日:2012-08-21
标题 :Haptens of olanzapine
发明人：DONAHUE MATTHEW GARRETT; GONG YONG; SALTER RHYS; HRYHORENKO ERIC; DECORY THOMAS R; REMMERIE BART; SANKARAN BANUMATHI
权利人:JANSSEN PHARMACEUTICA NV; ORTHO CLINICAL DIAGNOSTICS INC
摘要:The invention relates to compounds of Formula I, wherein R 1 , R 2 , and R 3 are defined in the specification, useful for the synthesis of novel conjugates and immunogens derived from olanzapine. The invention also relates to conjugates of an olanzapine hapten and a protein.