共查询到20条相似文献,搜索用时 15 毫秒
1.
Yu. A. Manaev V. P. Perevalov M. A. Andreeva B. I. Stepanov 《Chemistry of Heterocyclic Compounds》1986,22(3):265-267
The reaction of 4-bromo-1-methyl-3-nitropyrazole-5- and 4-bromo-1-methyl-5-nitro-pyrazole-3-carboxylic acids with arylamines in aqueous solution in the presence of monovalent copper salts leads to the formation of 4-arylamino- and 4-hydroxy substituted nitropyrazolecarboxylic acids.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 328–330, March, 1986. 相似文献
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Mark Pichowicz 《Tetrahedron》2010,66(13):2398-2403
4-Amino-3,5-dihalopyridines have been efficiently prepared via microwave-assisted nucleophilic aromatic substitution of 3,4,5-trihalopyridines using 1-1.1 equiv of primary and secondary amines. The reaction is also applicable to electron rich arylamines. 相似文献
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I. A. Nizova V. P. Krasnov O. V. Korotovskikh L. V. Alekseeva 《Russian Chemical Bulletin》1989,38(12):2545-2549
Reaction of p-substituted arylamines with dimethyl (2S,4RS)-4-bromo-N-phthaloy-1-glutamate followed by separation of the stereoisomers has given the pure dimethyl (2S)-4-arylamino-N-phthaloylglutamates. Nucleophilic replacement of the halogen in dimethyl (2S,4RS)-4-bromo-N-phthaloylglutmate is diastereoselective, giving the threo-isomer preferentially.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 12, pp. 2781–2785, December, 1989. 相似文献
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The Buchwald-Hartwig Pd-catalyzed C-N coupling reaction of 5-substituted 3-chloro-4H-1,2,6-thiadiazin-4-ones with primary (het)arylamines is described, affording twenty new 3,5-disubstituted 4H-1,2,6-thiadiazin-4-ones in 56–99% yield. The protocol enables the mild preparation of difficult to access 3,5-dianilino-1,2,6-4H-thiadiazin-4-ones. The reaction scope and limitations are discussed. 相似文献
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Conversion of propargyl alcohols to chloroallenes and arylalkynes using the TiCl4/R3N reagent system
Whereas the reaction of certain propargyl alcohols with TiCl4 in the presence of tertiary alkylamines gives the corresponding chloroallenes in 37-58% yields, reaction with the tertiary arylamines gives the corresponding arylalkynes in 68-77% yields. 相似文献
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Mariappan PeriasamyN. KishoreBabu Keela Natarajan Jayakumar 《Tetrahedron letters》2003,44(50):8939-8941
The reactions of arylacetic acid esters with tertiary arylamines in the presence of TiCl4 give α-arylated products in 65-90% yields, as well as 10-20% yields of the corresponding benzidines. 相似文献
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A. T. Soldatenkov T. P. Khristoforova A. W. Temesgen B. N. Anissimov B. B Averkiev L. N. Kuleshova V. N. Khrustalev M. Yu. Antipin 《Chemistry of Heterocyclic Compounds》2001,37(6):715-722
On treating 4-aryl substituted 1-methyl-1,2,3,6-tetrahydropyridines with potassium permanganate in the presence of arylamines a previously unknown intermolecular oxidative imination reaction occurs leading to the formation of 2-(arylimino)-1,2,5,6-tetrahydropyridines. The molecular structure of 1-methyl-2-(4-nitrophenylimino)-4-phenyl-1,2,5,6-tetrahydropyridine was studied by X-ray analysis and it was shown that the hydropyridine ring of the molecule has a sofa conformation and its amidine fragment is in the E-configuration. 相似文献
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An efficient and practical procedure was developed to prepare novel 2-(arylmethyl)amino-4-arylamino-6-alkyl-1,3,5-triazines, starting from dicyandiamide and the corresponding arylamines under microwave irradiation and its scope is demonstrated with a number of examples. The valuable feature of this procedure included the short reaction times, high yields, and easy operation. 相似文献
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N. Yu. Gorobets A. V. Borisov A. V. Silin V. M. Nikitchenko S. N. Kovalenko 《Chemistry of Heterocyclic Compounds》2002,38(11):1389-1396
The reaction of 3-(4-aryl-2-thiazolyl)- and 3-(2-benzothiazolyl)-2-iminocoumarins with N-nucleophiles was studied. This reaction gives 2-N-substituted 3-(4-aryl-2-thiazolyl)- and 3-(2-benzothiazolyl)iminocourmarins. N-Nucleophiles such as arylamines, heterocyclic amines, and hydrazine derivatives undergo this reaction. 相似文献
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Marjanović B Juranić I Cirić-Marjanović G 《The journal of physical chemistry. A》2011,115(15):3536-3550
New computational insights into the mechanism of the Boyland-Sims oxidation of arylamines with peroxydisulfate (S(2)O(8)(2-)) in an alkaline aqueous solution are presented. The key role of arylnitrenium cations, in the case of primary and secondary arylamines, and arylamine dications and immonium cations, in the case of tertiary arylamines, in the formation of corresponding o-aminoaryl sulfates, as prevalent soluble products, and oligoarylamines, as prevalent insoluble products, is proposed on the basis of the AM1 and RM1 computational study of the Boyland-Sims oxidation of aniline, ring-substituted (2-methylaniline, 3-methylaniline, 4-methylaniline, 2,6-dimethylaniline, anthranilic acid, 4-aminobenzoic acid, sulfanilic acid, sulfanilamide, 4-phenylaniline, 4-bromoaniline, 3-chloroaniline, and 2-nitroaniline) and N-substituted anilines (N-methylaniline, diphenylamine, and N,N-dimethylaniline). Arylnitrenium cations and sulfate anions (SO(4)(2-)) are generated by rate-determining two-electron oxidation of primary and secondary arylamines with S(2)O(8)(2-), while arylamine dications/immonium cations and SO(4)(2-) are initially formed by two-electron oxidation of tertiary arylamines with S(2)O(8)(2-). The subsequent regioselectivity-determining reaction of arylnitrenium cations/arylamine dications/immonium cations and SO(4)(2-), within the solvent cage, is computationally found to lead to the prevalent formation of o-aminoaryl sulfates. The formation of insoluble precipitates during the Boyland-Sims oxidation of arylamines was also computationally studied. 相似文献
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Starting from commercially available 4-amino-2,6-dichloropyrimidine, a practical four steps synthesis of 2-dialkylamino-4-arylamino-6-aminopyrimidines was developed. This strategy could introduce a diverse set of secondary amines and arylamines to displace the 2- and 4-chloro groups. The products of this route are otherwise difficult to access. In addition, 6-amino arylation was carried out to demonstrate the reactivity and utility of 2-dialkylamino-4-arylamino-6-aminopyrimidines as building blocks for assembling interesting aminopyrimidine molecules. 相似文献
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IntroductionAsoneofthemostimportantC—Cformationreactionsandone stepmethodforthearylationofolefins ,Heckre actionhasattractedmuchinterest.1However ,thereactionusuallyneedsarelativelylargeamountofpalladiumcata lyst (>1mol%)forsatisfactoryconversions .Recently ,avarietyofpalladacyclesincorporatingcyclometallatedphos phine ,2 phosphite ,3 carbene ,4 imine5andoxime6havebeenreported .Theuseofcatalystswithnitrogen basedligandswasdemonstratedtopossessveryhighactivity .Wehavereportedthecyclopalladat… 相似文献
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An efficient synthetic method for 4-functionalized quinoline derivatives, 4-((1,3-dithian-2-ylidene)methyl)quinolines, has been developed. Mediated by trifluoromethanesulfonic acid, ethynyl ketene-S,S-acetals can react in a one-pot procedure with various arylamines and aldehydes under mild conditions to give the corresponding quinoline derivatives in good to high yields via a consecutive arylimine formation, regiospecific aza-Diels-Alder (Povarov) reaction, and reductive amination. 相似文献
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I. N. Fesun V. M. Timoshenko Yu. G. Shermolovich 《Russian Journal of Organic Chemistry》2006,42(2):261-265
Reactions of 4-fluoro-5-polyfluoroalkyl-1,2-dithiol-3-thiones with hydroxylamine and hydrazines occur with replacement of the thiocarbonyl by imino group affording oximes and hydrazones respectively. N-Alkyl-and N-aryl-3-imino-1,2-dithiolenes formed in reactions of 3-chlorothio-1,2-dithiolium salts with primary alkyl-or arylamines. 3-Chlorothio-1,2-dithiolium salts react with compounds possessing an active methylene group yielding 3-ylideno derivatives of 1,2-dithiolenes. 相似文献
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N. A. Burmistrova S. P. Mushtakova P. E. Kuznetsov 《Journal of Analytical Chemistry》2006,61(12):1183-1186
It is demonstrated that 4-dimethylaminochalcone (DMC) can be used as a fluorescent probe for studying the microenvironment in the arylamine-surfactant system. A molecular simulation of the location of DMC at the water-lipophilic medium phase boundary is performed. The fluorescence of DMC is studied in aqueous solutions of dimethylformamide and surfactants of different natures. The influence of the nature and concentration of arylamines on the characteristics of the fluorescence of DMC in micellar TX-100 solutions is revealed. 相似文献
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N. M. Igidov A. E. Rubtsov A. V. Tyuneva V. V. Zalesov A. Yu. Borodin E. V. Bukanova 《Russian Journal of Organic Chemistry》2009,45(5):698-704
Reactions of arylamines with 4-aryl-2-hydroxy-4-oxobut-2-enoic and 2-hydroxy-5,5-dimethyl-4-oxohex-2-enoic acids gave rise to 4-aryl-2-arylamino-4-oxobut-2-enoic and 2-aryl-amino-5,5-dimethyl-4-oxohex-2-enoic acids that existed in solutions as Z- and E-isomers or in a ring form as 3-arylamino-5-tert-butyl-5-hydroxyfuran-2(5H)-ones. The probable cyclization mechanism of these compounds into 5-R-3-arylimino-3H-furan-2-one derivatives was considered. 相似文献
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芳香胺参加的Mannich反应——3-芳氨基-3-苯基-1-(4-溴苯基)丙酮的合成 总被引:2,自引:0,他引:2
文献报道过芳香胺与苯甲醛生成的Schiff碱可在少量相应的芳香胺盐酸盐或浓盐酸催化下制备Mannich碱(Ⅰ),所用的Schiff碱系事先合成,且产率较低(15-68.9%)。本文报导用4-溴苯乙酮、苯甲醛和芳香胺在少量浓盐酸催化下能直接发生Mannich反应, 相似文献
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Activated aryl halides undergo smooth nucleophilic substitution reactions with secondary amines in 1-butyl-3-methylimidazolium hexafluorophosphate ([bmim]PF6) or 1-butyl-3-methylimidazolium tetrafluoroborate ([bmim]BF4) ionic liquids (ILs) at room temperature to afford the corresponding arylamines in excellent yields under mild and neutral conditions. 相似文献