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Synthesis of 2-Arylimidazo[1, 2-a]pyrimidines in Ionic Liquids 总被引:1,自引:0,他引:1
DanQianXU BaoYouLIU ZhenYuanXU 《中国化学快报》2003,14(10):1002-1004
Room temperature ionic liquids were used as a “green“ recyclable alternative to conventional solvents in the synthesis of pharmaceutically useful compounds 2-arylimidazo[1, 2-a]pyrimidines through Tschotschibabin reaction of a-bromoacetophenones with 2-aminopyrimidine in good yields. 相似文献
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Dan Qian XU Bao You LIU Zhen Yuan XU Catalytic Hydrogenation Research Center Zhejiang University of Technology Hangzhou 《中国化学快报》2003,(10)
Room temperature ionic liquids were used as a "green" recyclable alternative to conventional solvents in the synthesis of pharmaceutically useful compounds 2-arylimidazo[1, 2-a] pyrimidines through Tschotschibabin reaction of a-bromoacetophenones with 2-aminopyrimidine in good yields. 相似文献
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The reactions of (2S)-2-amino-2-substituted-N-(4-nitrophenyl)acetamides 16a-c, succindialdehyde (13), and benzotriazole afforded enantiopure (3S,5R,7aR)-5-(1H-1,2,3-benzotriazol-1-yl)-3-substituted-1-(4-nitrophenyl)tetrahydro-1H-pyrrolo[1,2-a]imidazol-2-ones 17a-c, which were converted by sodium borohydride into (3S,7aR)-3-substituted-1-(4-nitrophenyl)tetrahydro-1H-pyrrolo[1,2-a]imidazol-2-ones 18a-c. Chiral (2S)-2-amino-2-substituted-N-(4-methylphenyl)acetamides 12a-d, easily prepared in two steps from N-Boc-alpha-amino acids 10a-d, similarly reacted with glutaraldehyde (20) and benzotriazole to generate 5-benzotriazolyl-3-substituted-hexahydroimidazo[1,2-a]pyridin-2(3H)-ones 21a-d, which were converted by sodium borohydride directly into optically active 3-substituted-hexahydroimidazo[1,2-a]pyridin-2(3H)-ones 22a-d. 相似文献
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《Mendeleev Communications》2023,33(2):164-166
Acetylene reacts with 2-aminopyridines in the superbase system KOBut/DMSO (the initial acetylene pressure ∼8 atm, 80 °C, 5 min) to give 2,3-dimethylimidazo[1,2-α]-pyridines in up to 60% yields. In the case of 2-amino-5-chloropyridine, along with ‘normal’ product, (Z)-5-chloro- N-[2-(2,3-dimethylimidazo[1,2-α]pyridin-6-yl)vinyl]pyridin-2-amine is formed in 40% yield. These multi-molecular assemblies involve parallel nucleophilic addition of N-centered anions to the triple bond and ethynylation of the forming C=N bond. 相似文献
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A. P. Krapivko E. A. Savitkina Kuanu A. Antares A. A. Astakhov A. V. Varlamov 《Chemistry of Heterocyclic Compounds》1996,32(3):290-293
Reductive cyclization of 1-(2,4-dinitrophenyl)-3-methyl-4-dimetkylphenyisililpyridinium chloride by the action of phenylkydrazine or hydrogen in the presence of Pd/C gave, for the first time, 7-nitro (amino)-3 dimethylphenylsilylpyrido[l, 2-affienzimidazoles.Russian University of the Friendship of Nations, Moscow, 117923. Translated from Khimiya Geterots ikl icheskikh Soedinenii, No, 3, pp. 338–341, March, 1996. Original article submitted November 27, 1995. 相似文献
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Chemistry of Heterocyclic Compounds - 相似文献
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Sokolov V. B. Aksinenko A. Yu. Epishina T. A. Goreva T. V. 《Russian Chemical Bulletin》2009,58(3):631-633
3-Fluoro-2-trifluoromethylimidazo[1,2-a]pyridines were obtained by reactions of hexafluoroacetone 2-pyridylimines with trimethyl phosphite and studied in reactions
with sodium methoxide. This gave the corresponding 3-methoxy-2-trifluoromethylimidazo[1,2-a]pyridines. 相似文献
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The synthesis and characterisation of some of the new pyrido [1,2-a] benzimidazoles from 1H-benzimidazole-2-acetonitrile and diethyl ethoxy methylene malonic ester. 相似文献
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S. M. Desenko V. D. Orlov V. V. Lipson O. V. Shishkin S. V. Lindeman Yu. T. Struchkov 《Chemistry of Heterocyclic Compounds》1993,29(5):588-592
The oxidation of aromatic derivatives of 1,4- and 3,4-dihydropyrimido[1,2a]benzimidazoles gave the corresponding 3-hydroxy-3,4-dihydro derivatives and the dehydrogenation of these compounds was carried out. An x-ray diffraction structural analysis was carried out on 2-(4-dimethylaminophenyl)-3-hydroxy-4-phenyl-3,4-dihydropyrimido[1,2a]benzimidazole.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 688–693, May, 1993. 相似文献
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2-乙酰基吡啶1经溴化反应后得到2-(2-溴乙酰基)吡啶氢溴酸盐2,2在水中与NaHCO3发生中和反应生成2-(2-溴乙酰基)吡啶,不经分离直接于水中和2-氨基吡啶衍生物3a-3h反应生成2-吡啶基咪唑并[1,2-a]吡啶4a-4h.采用核磁共振谱仪、红外光谱仪及质谱仪表征了产物的结构.结果表明,利用该方法可以在温和的反应条件下高产率得到目标产物,且方法操作简便、对环境友好. 相似文献
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The alkylation of 2-chloroindole-3-carboxaldehyde ( 1 ) and 3-acetyl-2-chloroindole ( 5 ) with 3-chloro-N,N-dimethyl-1-propylamine, 3-chloro-N,N-diethyl-1-propylamine and 2-chloro-N,N-dimethyl-1-ethylamine is described. Following alkylation, demethylation occurs and furnishes imidazo[1,2,-a]- and pyrimido[1,2-a]indoles ( 3a,6,8,10 ). Pyrimido-indole 3a , on treatment with lithium aluminum hydride, furnishes the bis-indole 12 . Analogous reaction with diborane affords the reduced product 14 , while reaction with methyllithium yields the deformylated product 13 . Spectral data of the resulting compounds are also discussed. 相似文献