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1.
We have prepared the pyrrolopyridazines 7a-f starting from the diazo compounds 4 . The synthesis involves a tandem condensation-aza-Wittig reaction or a combination of Wittig and aza-Wittig reactions as key steps. Reaction of pyridazine 7d with diazomethane results in C-methylation to yield 7g . Sodium borohydride reduces 7d to either the dihydropyridazine 12 or the hydroxylactam 13b depending of the reaction conditions. 相似文献
2.
Sanchez-Martinez C Faul MM Shih C Sullivan KA Grutsch JL Cooper JT Kolis SP 《The Journal of organic chemistry》2003,68(21):8008-8014
Synthesis of aryl- and hetero[a]pyrrolo[3,4-c]carbazoles by photochemical oxidation and Heck cyclization are described. Photochemical oxidation of 2-naphthyl indolyl maleimide affords two different carbazole regioisomers, depending on the reaction conditions. The regiochemistry of the cyclization can be controlled using the Heck reaction. 相似文献
3.
Dario Giardina Roberto Ballini Marcello Ferappi Giovanni Casini 《Journal of heterocyclic chemistry》1978,15(6):993-995
The: title compounds were prepared from Michael adducts, obtained from acetoacetic esters and trans-3-hexene-2,5-dione, and from the corresponding dehydration products, by direct cyclization to oxygen rings or by reaction with ammonia (or methylamine) to give nitrogen rings. 相似文献
4.
Shuntaro Mataka Kazufumi Takahashi Masashi Tashiro 《Journal of heterocyclic chemistry》1981,18(6):1073-1075
The reaction of 3,4-dibenzoyl-1-methyl-2,5-diphenylpyrrole ( 1 ) and -1-phenylpyrazole ( 2 ) with methylamines ( 3a-c ) afforded pyrrolo[3,4-c]pyridine ( 4 ), and isomeric 2H-pyrazolo[3,4-c]pyridines ( 5a-c ) and [4,3-c]pyridines ( 6a-c ), respectively. 相似文献
5.
S. V. Fedoseev O. V. Ershov M. Y. Belikov K. V. Lipin O. E. Nasakin V. A. Tafeenko 《Russian Journal of Organic Chemistry》2013,49(11):1661-1665
Reactions of 3-amino-8-hydroxy-1,6-dioxo-2,7-diazaspiro[4.4]non-3-ene-4-carbonitriles with aqueous hydrohalic acid led to the formation of alkyl-substituted pyrrolo[3,4-c]-pyrrole-1,3,4,6-tetraones. 相似文献
6.
7.
A. Shafiee M. A. Ebrahimzadeh J. Shahbazi S. Hamedpanah 《Journal of heterocyclic chemistry》1998,35(1):71-75
Starting from the readily available aryl 2-methyl-5-phenyl-3-furyl ketones, 5-methyl-1H-1-phenylpyrazole-4-yl ketones and 4-methyl-2-phenyl-5-thiazolylcarboxaldehyde, a series of 2-phenyl-4-arylthieno[3,4-b]-furan, 2-phenyl-4-(p-methoxyphenyl)selenolo[3,4-b]furan, 4-aryl-1H-1-phenylthieno[3,4-c]pyrazole and 5-benzyl-2-phenylpyrrolo[3,4-d]thiazole were prepared in high yield. 相似文献
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10.
F. A. Amer M. Hammouda A.-A. S. El-Ahl B. F. Abdel-Wahab 《Chemistry of Heterocyclic Compounds》2007,43(12):1559-1566
New pyrrolo[3,4-c]isoxazole derivatives were synthesized from the key intermediates 4-cyanopyrrolidin-3-ones in two steps.
Pyrrolo[2,3-d][1,2,3]triazoles and triazolo[4,5-c]pyridazine were obtained from 2-arylhydrazono-4-cyano-1-(4′-methoxyphenyl)-3-oxopyrrolidines
by refluxing with phenylhydrazine in either ethanol or glacial acetic acid. Aldol self-condensation of 1-aryl-4-cyanopyrrolidin-3-ones
afforded dipyrrolo-[3,2-b:3′, 4′-d]pyran derivatives.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 12, pp. 1841–1848, December, 2007. 相似文献
11.
Pyrrolo[2,1-c][1,2,4]benzothiadiazines have been prepared from the reactions of o-amino-benzenesulfonamides with γ-cyanopropionaldehydes. Pyrrolo[1,2-a]quinazolines have been prepared from the reaction of anthranilamides with either γ-cyanopropionaldehyde or succinic anhydride. The cyclization of a 4-oxo-2-quinazolinepropionic acid has produced a pyrrolo-[1,2-a]quinazoline and the isomeric pyrrolo[2,1-b]quinazoline. 相似文献
12.
The base promoted four-component reaction of hydrated hydrazine, dimethyl acetylenedicarboxylate, isatines and malononitrile (ethyl cycanoacetate) in ethanol afforded polysubstituted spiro[indoline-3,4‘-pyrano[2,3-c]pyrazoles] and spiro[acenaphthyl-3,4-pyrano[2,3-c]pyrazoles] 相似文献
13.
S. A. Yamashkin N. Ya. Kucherenko M. A. Yurovskaya 《Chemistry of Heterocyclic Compounds》1995,31(11):1299-1301
It is shown that the reaction of 2, 3, 5-trimethyl-6-amino-indole with 1, 3-diketones is a convenient method for the preparation of angular IH-pyrrolo[2,3-f]quinolines, while the presence of a methyl group on the pyrrolic nitrogen atom of the initial indole as a result of steric hindrance completely blocks cyclization to the corresponding pyrroloquinolines.Mordovskii State Educational Institute, Saransk 430007. Moscow State University, Moscow 119899. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No 11, pp. 1499–1501, November, 1995. Original article submitted May 23, 1995. 相似文献
14.
Acylation of 3-acetonyl- and 3-phenacyl-2,5-dimethylthiophenes with aliphatic acid anhydrides in the presence of perchloric acid gives thieno[3,4-c]pyrylium perchlorates. Reaction of the latter with ammonia gives the corresponding thieno[3,4-c]pyridines or diketones of the thiophene series. Selenopheno[3,4-c]pyrylium salts could not be isolated in the acylation of 3-acetonyl- and 3-phenacyl-2,5-dimethylselenophenes. 相似文献
15.
The fragmentation behaviour of some [1]benzopyrano[3,4-c]pyrazole and [1]benzopyrano[4,3-d]isoxazole derivatives under electron impact is described. 相似文献
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17.
V. M. Dziomko B. K. Berestevich R. S. Kuzanyan 《Chemistry of Heterocyclic Compounds》1979,15(6):654-656
The substance isolated from the template cyclization of 4-(2-bromo-4-methyl-1-phenylazo)-5-amino-3-methyl-1-propylpyrazole was identified by spectroscopic methods as 5-(2-bromo-4-methylphenyl)-3,7-dimethyl-1-propyl-1,5-dihydrobenzo[f]-pyrazolo[3,4-c][1,2,5]triazepine.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 802–804, June, 1979. 相似文献
18.
p-TsOH catalyzed Diels-Alder reaction of 3-(indol-3-yl)maleimides with 3-phenacylideneoxindoles in toluene at 80 °C for two hours afforded cis/trans isomers of 3a',4′,6′,10c'-tetrahydrospiro[indoline-3,5′-pyrrolo[3,4-c]carbazoles] in nearly comparable yields, which could be easily converted to the corresponding 4′,6′-dihydrospiro[indoline-3,5′-pyrrolo[3,4-c]carbazole] in high yields and with high diastereoselectivity by further DDQ oxidation. Additionally, the similar reaction of 3-(indol-3-yl)maleimides with 2-arylidene-1,3-indanediones in toluene 80 °C and sequential DDQ oxidation afforded functionalized dihydrospiro[indene-2,5′-pyrrolo[3,4-c]carbazoles] as major products. 相似文献
19.
T. N. Borisova A. é. Aliev I. A. Stazharova N. S. Prostakov A. V. Varlamov 《Chemistry of Heterocyclic Compounds》1991,27(6):671-671
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 849–850, June, 1991. 相似文献
20.
E. E. Stashenko P. I. Zakharov T. N. Borisova A. V. Varlamov B. S. Subbotin N. S. Prostakov 《Chemistry of Heterocyclic Compounds》1988,24(2):176-179
The dissociative ionization of derivatives of pyrrolo[3,2-c]piperidines and their deutero analogs was studied. The successive elimination of the substituents in the piperidine ring, which leads to its aromatization, and cleavage of this ring via a retrodiene fragmentation mechanism are the principal pathways of fragmentation of these substances. The principles found make it possible to determine the position and character of the substituents in the piperidine ring of derivatives of pyrrolo[3,2-c]piperidines.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 212–215, February, 1988. 相似文献