共查询到20条相似文献,搜索用时 31 毫秒
1.
Srinivas Kantevari C. K. Snehalatha Nair M. Pardhasaradhi 《Journal of heterocyclic chemistry》2006,43(5):1353-1356
Practical synthesis of 5‐(4′‐methylbiphenyl‐2‐yl)‐1H‐tetrazole, key intermediate in several angiotensin II receptor antagonists from 2‐fluorobenzonitrile in excellent yields and very high purity is described. 相似文献
2.
Martial Say Ekaterina Paliakov Maged Henary Lucjan Strekowski 《Journal of heterocyclic chemistry》2006,43(6):1613-1620
Facile synthetic approaches to 2‐phenylquinolin‐4‐amines containing an aminoalkyl group at N4 of the quinolin‐4‐amine and amino or aminoalkyl groups at the phenyl moiety are presented. 相似文献
3.
Several 4‐substituted‐3, 5‐bis(2‐pyridyl)‐1H‐pyrazoles, where the substituent is chloro, bromo, iodo, nitro, diazo, were synthesized under mild reaction conditions in high yields. The structures of the products were characterized by 1H NMR, 13C NMR, ESI‐MS, IR and elemental analyses. 相似文献
4.
The title aldehyde 1 reacts smoothly with the enamine moiety of 2 ‐aminochromone 2 to produce hitherto unreported 3‐(2‐hydroxybenzoyl)‐5H‐1‐benzopyrano[2,3‐b]pyridin‐5‐one (azaxanthone) 5 . This reaction has been extended for the synthesis of bisazaxanthone 9. 相似文献
5.
E. S. H. El Ashry A. A. Kassem H. Abdel‐Hamid F. F. Louis S. H. A. N. Khattab M. R. Aouad 《Journal of heterocyclic chemistry》2006,43(6):1421-1429
Under microwave irradiation (MWI), 5‐(3‐chlorobenzo[b]thien‐2‐yl)‐4H‐1,2,4‐triazole‐3‐thiol ( 3 ) was synthesized in a good yield by intramolecular cyclization of the carbonyl thiosemicarbazide 2. A regioselective S‐alkylation of 3 with benzyl chloride or allyl bromide has been achieved by using triethylamine as a base, while other different basic conditions led to a mixture of bis(alkylated) derivatives N4, S‐ and S, N2‐, under both of classical and MWI conditions. The relative stabilities, charge densities, dipole moments and electronic energies of reactants, transition states and intermediates were calculated by the AM1 method and used for investigating the regioselectivity. 相似文献
6.
The paper describes the synthesis of new 1,3,3‐triary‐1′‐methylspiro[azetidine‐2,3′‐indoline]‐2′,4‐diones from reaction of the 2‐diazo‐1,2‐diarylethanones with 3‐arylimino‐1‐methyl‐2‐indolinones. The compounds have been characterized by satisfactory analytical and spectral (IR, 1H NMR and 13C NMR) data. The diarylketenes, generated in situ from thermal decomposition of the 2‐diazo‐1,2‐diarylethanones, react with azomethine linkage in preference to carbonyl group leading to the formation of products. 相似文献
7.
Sivaperuman Saravanan Arumugam Nithya Shanmugam Muthusubramanian 《Journal of heterocyclic chemistry》2006,43(1):149-155
The synthesis of a new set of selenadiazoles, 4‐aryl‐5‐(1‐aryl‐2‐methyl‐2‐nitropropyl)‐1,2,3‐selenadiazoles ( 4 ) derived from 2‐[4‐methyl‐4‐nitro‐1,3‐diarylpentylidene]‐1‐hydrazinecarboxamide ( 3 ) has been reported. THF has been found to be the solvent of choice for this reaction. Structural features of 3 and 4 have been analyzed by NMR and X‐ray techniques. 相似文献
8.
A. V. Karnik N. J. Malviya A. M. Kulkarni D. Jaimini B. L. Jadhav 《Journal of heterocyclic chemistry》2006,43(2):489-493
Chemoselective synthesis of novel hetero cyclopenta[b]chrysene derivatives, namely, 6‐Aryl‐2,2a‐dihydro‐naphtho[2′,1′‐5,6]pyrao[4,3‐e][1,2,4]triazolo[3,4‐b][1,3,4]thiadiazine ( 4a‐j ) under neutral condition has been described. These molecules exhibited good to excellent anti‐bacterial activities. 相似文献
9.
Vladimir V. Kouznetsov Diego F. Amado Ali Bahsas Juan Amaro‐Luis 《Journal of heterocyclic chemistry》2006,43(2):447-452
New αω‐bis‐(2‐hetaryl‐4‐oxothiazolidin‐3‐yl)alkanes were prepared via a common two step procedure using N,N‐bis‐hetarylidenamines condensation with α‐mercaptoacetic acid. The used bis‐aldimines were obtained from reaction between ethylenediamine or putrescine and benzaldehyde or the isomeric pyridinecarboxyaldehydes. The bis‐(2‐phenyl‐4‐oxothiazolidin‐3‐yl)alkanes were prepared by one‐pot three component reaction of diamine, aldehyde and α‐mercaptoacetic acid under very mild conditions. 相似文献
10.
Xinglong Jiang Guang‐Pei Chen Kapa Prasad Oljan Repi
Thomas J. Blacklock 《Journal of heterocyclic chemistry》2006,43(6):1725-1728
A general method for the synthesis of 8‐hydroxy‐6‐substituted‐1,7‐naphthyridines is described using acylation of the dianion derived from tert‐butylamide 1 , followed by cyclization of the resulting intermediate ketones 2 with ammonium acetate. 相似文献
11.
Shujiang Tu Qian Wang Jianing Xu Xiaotong Zhu Jinpeng Zhang Bo Jiang Runhong Jia Yan Zhang Junyong Zhang 《Journal of heterocyclic chemistry》2006,43(4):855-858
A series of 5‐aryl substituted 2‐amino‐5,8‐dihydropyrido[2,3‐d]pyrimidin‐4,7‐diones were synthesized through one‐pot condensation of 2,6‐diaminopyrimidin‐4‐one, aldehyde and Meldrum's acid using glycol as energy transfer agent under microwave irradiation without catalyst. The one‐pot protocol in the absence of catalyst has the advantage of good yield (86‐95%), short route and reaction time (3‐6 min) and environmentally friendly. 相似文献
12.
Regina Janciene Zita Stumbreviciute Daiva Podeniene Benedikta D. Puodziunaite Steve Black Stephen M. Husbands 《Journal of heterocyclic chemistry》2006,43(4):979-984
A number of substituted 4H,5H,6H‐thiazolo[3,2‐a][1,5]benzodiazepinium salts 2a‐h, 5, 9 , which are based on the novel thiazolobenzodiazepine system, were prepared by condensation‐cyclization of 1,5‐benzodiazepine‐2‐thiones 1a‐f, h, 4 with α‐haloketones, as well as with α‐bromoacetaldehyde diethyl acetal. The structure and stereochemistry of the ring system obtained were investigated by 1H and 13C nmr spectroscopy: the additional heterocyclic nucleus was found to appreciably influence the conformational mobility of the heptatomic ring. Upon treatment of salt 2d with alkali the presence of the base enamine structure in solution has been postulated. 相似文献
13.
The reaction of camphoraniles 3a,b with “magic malonates” (bis‐2,4,6‐trichlorophenylmalonates) 4a,b leads to 4‐hydroxy‐2(1H)‐pyridones attached to bornane ring system 6a‐c in good yields. Less satisfactory yields were obtained with the diethyl malonate 5b . The reaction of an excess of diethyl malonate 5 itself with 3b yields the pyrono derivative 7 , which can readily be degraded via the acetyl derivative 8 to the basic structure 9 . 相似文献
14.
Milda M. Burbuliene Olegas Bobrovas Povilas Vainilavicius 《Journal of heterocyclic chemistry》2006,43(1):43-47
Treatment of ambident sodium salt of 2‐methylsulfanyl‐4(3H)‐quinazolinone with methyl bromoacetate resulted in N(3)‐alkyl ester formation. Reaction of the resulted ester with hydrazine hydrate gave 2‐methylsulfanyl‐4‐oxo‐3(4H)‐quinazolinyl)acetohydrazide, which underwent intramolecular cyclization under heating in dimethylformamide to give 1‐aminoimidazo[2,1‐b]quinazoline‐2,5(1H,3H)‐dione. The latter took place in acylation reaction and in condensation with aromatic aldehydes. 相似文献
15.
Jií Hanusek Pavel Drabina Milo Sedlk Pavel Rosa 《Journal of heterocyclic chemistry》2006,43(5):1281-1285
Acylation of 2‐amino‐N‐methyl‐thiobenzamide with substituted benzoyl chlorides has been used to synthesize the corresponding 2‐benzoylamino‐N‐methylthiobenzamides. Subsequent sodium methoxide‐catalyzed ring closure gives the corresponding 3‐methyl‐2‐phenylquinazoline‐4‐thiones. These compounds were characterized by means of their 1H‐ and 12C‐NMR spectra. The kinetics of the cyclization reaction has been followed with UV‐VIS spectroscopy at 100 °C in methanolic solutions of sodium methoxide. 相似文献
16.
17.
Dijana Pei Ivana Ozimec Landek Mladen Meraep Milan Mesia 《Journal of heterocyclic chemistry》2006,43(3):749-754
A novel synthetic route to 2‐methyl‐1,8‐dioxa‐dibenzo[e,h]azulenes [1] via cyclisation of the corresponding 1,4‐dicarbonyl compound is described. 1,4‐Dicarbonyl compounds were synthesized by the alkylation reaction of the 11H‐dibenzo[b,f]oxepine‐10‐one while analogous alkylation of 11H‐dibenzo[b,f]thiepine‐10‐one resulted in formation of O‐alkylated products. Selective oxidation of 2‐methyl group afforded 1,8‐dioxa‐dibenzo[e,h]azulenes with formyl and hydroxymethyl functionality at C(2) position. 相似文献
18.
Gerardo Blanco Jos M. Quintela Carlos Peinador 《Journal of heterocyclic chemistry》2006,43(4):1051-1056
An efficient one‐pot access for the synthesis of the previously unreported tetracyclic fused pyrimido‐[4″,5″:4′,5′]thieno[3′,2′:4,5]thieno[3,2‐d]pyrimidine ( 3 ) and 1,2,3‐triazine[4″,5″:4′,5′]thieno‐[3′,2′:4,5]thieno‐[3,2‐d]‐1,2,3‐triazine ( 5 ) heteroaromatic nitrogen ligands is described. The title compounds 3 and 5 were obtained from 3,4‐diaminothieno[2,3‐b]thiophene‐2,5‐dicarbonitrile and phosgeniminium chloride and sodium nitrite/HCl, respectively. Substituted condensed thieno[2,3‐b]thiophene derivatives 4 and 6 were synthesized by nucleophilic displacement of the chloroderivatives 3 and 5 . 相似文献
19.
Giuseppe Granata Salvatore Barbagallo Antonio Perdicaro Agostino Marrazzo Andrea Santagati Laura Lombardo Venera Cardile 《Journal of heterocyclic chemistry》2006,43(4):1099-1104
Methane sulfonamide derivatives of 3‐amino‐2‐thioxo‐2,3‐dihydrothieno[2,3‐d]pyimidin‐4(1H)‐one, potential selective COX‐2 inhibitors, were synthesized and their structural elucidation is here reported. Some derivatives, at 10 μM concentration, showed a significant percentage of inhibition in some in vitro experiments. 相似文献
20.
Girija S. Singh 《Journal of heterocyclic chemistry》2006,43(6):1653-1656
The reaction of 2‐diazo‐1,2‐diarylethanones with benzophenone N‐(diaryl)acyl hydrazones leads to the formation of 1,3,4‐oxadiazolines. The products have been characterized on the basis of satisfactory analytical and spectral (IR, 1H and 13C NMR, and Mass) data. The mechanism for the formation of products through the reaction of diarylketenes, generated in situ from thermal decomposition of the 2‐diazo‐1,2‐diarylethanones, with imino nitrogen and intramolecular [2 + 3] dipolar cycloaddition is suggested. 相似文献