共查询到20条相似文献,搜索用时 31 毫秒
1.
M. N. Armisheva N. A. Kornienko V. L. Gein M. I. Vakhrin 《Russian Journal of General Chemistry》2011,81(9):1893-1895
The reaction of 5-(4-chlorophenyl)-4-benzoyl-1-(4-hydroxyphenyl)-3-hydroxy-3-pyrrolin-2-one with aromatic amines affords the
corresponding 3-arylamino derivatives, and the reactions of 5-aryl-4-acetyl-1-(4-hydroxyphenyl)-3-hydroxy-3-pyrrolin-2-ones
with p-toluidine yield 5-aryl-4-(1-p-tolylamino)ethylene-1-(4-hydroxyphenyl)pyrrolidin-2,3-diones. 相似文献
2.
Sheng-Yin Zhao Bao-Shuo Liu Jing Huang Shao-Hua Cheng Yun-xia Deng Zhi-Yu Shao 《合成通讯》2014,44(14):2066-2075
Thermal-induced dimerization cyclization of ethyl N-(styrylcarbamoyl)acetate derivatives has been investigated, leading to 4-hydroxy-2(1H)-pyridone-3-carboxamide derivatives with good yields in diphenyl ether on 200–210 °C. Ethyl N-(styrylcarbamoyl)acetate derivatives readily provided the intermolecular cyclization products 4-hydroxy-2(1H)-pyridone-3-carboxylates on reflux in xylene. In addition, several related 3-acetyl-4-hydroxy-5-phenylpyridin-2(1H)-ones have been prepared. It provided an efficient preparation of 4-hydroxy-2(1H)-pyridone-3-carboxamide derivatives. 相似文献
3.
A. N. Grinev V. M. Lyubchanskaya L. S. Sarkisova L. M. Alekseeva Yu. N. Sheinker 《Chemistry of Heterocyclic Compounds》1986,22(1):18-22
The 2-, 6-, and 7-aminomethyl derivatives have been synthesized from derivatives of 4-hydroxy-5-methoxy- and 4-methoxy-4-hydroxybenzofuran. 2-Methyl-3-carbethoxy-5-methoxy-7-dimethylaminomethylbenzofuran has been converted into the 7-cyanomethyl derivative.Deceased.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 23–27, January, 1986. 相似文献
4.
L. D. Smirnov V. I. Kuz'min Yu. V. Kuznetsov 《Chemistry of Heterocyclic Compounds》2005,41(8):1013-1018
The aminomethylation of 3-hydroxy-6-methyl- and 3-hydroxy-2-(2-phenylethyl)pyridines by secondary amines has been investigated.
It was shown that like 2-alkyl-3-hydroxypyridine aminomethylation is directed primarily to position 6 and then 4 of the pyridine
ring. On heating the aminomethyl derivatives of 3-hydroxy-6-methyl- and 3-hydroxy-2-(2-phenylethyl)pyridines with acetic anhydride
the corresponding acetoxy derivatives were obtained, which were converted on heating with hydrochloric or hydrobromic acids
into hydroxy and bromomethyl derivatives. Isothioureidomethyl and benzimidazolylthiomethyl derivatives were synthesized by
heating the bromomethyl-substituted derivative with thiourea or with 2-mercaptobenzimidazole. The structures of compounds
were confirmed by data of 1H NMR spectra.
__________
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1189–1194, August, 2005. 相似文献
5.
《Tetrahedron》1961,16(1-4):30-44
1-(Cyclohexenyl- and 1-cycloheptenylnitromethane have been used as starting substances to yield 2-nitro-2-(1′-cyclohexenyl)- and 2-nitro-2-(1′-cycloheptenyl)-propanediol-1,3 (B) respectively. By reacting them with formaldehyde and benzylamine or formaldehydes and cyclohexylamine, derivatives of tetrahydro-1,3-oxazine (B) have been prepared. Acid hydrolysis of tetrahydro-1,3-oxazine derivatives results in the formation of 3-hydroxy-2-nitro-2-(1′-cyclohexenyl)- and 3-hydroxy-2-nitro-2-(1′-cycloheptenyl)-propylamine derivatives (E). Both aminoalcohols (E) react with formaldehyde to again yield tetrahydro-1,3-oxazine derivatives (C).
Infra-red spectra of C and E and their hydrochlorides D and F were examined and structure assignments made of the principal bands. 相似文献
6.
Italo Menconi E. Angeles Luisa Martínez Maria E. Posada Rubn A. Toscano Roberto Martínez 《Journal of heterocyclic chemistry》1995,32(3):831-833
The Hantzsch condensation of 2-hydroxy-5-nitrobenzaldehyde, ethyl acetoacetate and ammonia gave the hitherto unknown 2-methyl-3-ethoxycarbonyl-4-ethoxycarbonylmethyl-6-(2-hydroxy-5-nitrophenyl)-pyridine via an unusual condensation and oxidation in situ. 相似文献
7.
借处理2-羟基-5-(2-苯基-4-喹啉基)-1,3,二唑同PCl_5/POCl_3之间的反应合成了2-氯-5-(2-苯基-4-喹啉基)-1,3,4-二唑(3)和通过2-基-5-(2-苯基-4-喹啉基)-1,3,4-二唑的甲基化,然后氧化制得2-甲磺酰基-5-(2-苯基-4-喹啉基)-1,3,4-二唑(6).并分别研究了3和6同胺、叠氮及肼的反应,得到2,5-二取代的二唑新衍生物.初步观察了部分化合物的抗菌活性. 相似文献
8.
Z. G. Aliev A. N. O. L. Maslivets Yu. N. Bannikova L. O. Atovmyan 《Journal of Structural Chemistry》2003,44(4):707-710
1-Benzyl-4-benzoyl-5-phenyl-2,3-dihydro-2,3-pyrroledione reacts with ketene diethylacetal, forming 1-benzyl-4-benzoyl-3-hydroxy-5-phenyl-5-ethoxycarbonylmethyl-2,5-dihydro-2-pyrrolone, whose crystal and molecular structure was studied by XRD. 相似文献
9.
Alex F. C. Flores Juliana L. Malavolta Leandro M. Frigo Morgana Doneda Darlene C. Flores 《合成通讯》2013,43(10):1198-1204
We develop an efficient method to synthesize novel propionyl-spaced bisheterocyclic compounds. It entails cyclocondensation of 3-(5-trifluoromethyl-1H-pyrazol-3-yl)propanoyl hydrazide obtained from levulinic acid, with 1,1,1-trifluoro-4-methoxy-3-alken-2-ones proceeding regiospecifically to 1-[(5-trifluoromethyl-5-hydroxy-3-substituted-4,5-dihydro-1H-pyrazol-1-yl)-3-(5-trifluoromethyl-1H-pyrazol-3-yl)propan-1-one derivatives. 相似文献
10.
An unexpected product, 1-(4-ethoxycarbonylmethyl-5-nitro-2-furyl)-2-(2-furyl)-3-ethoxycarbonyl-indolizine was obtained by the reaction of α-(2-furyl)-β-(5-nitro-2-furyl)ethynyl with N-ethoxy-carbonylmethylpyridinium ylide in N,N-dimethylformamide, together with 1-(5-nitro-2-furyl)-2-(2-furyl)-3-ethoxycarbonylindolizine. 相似文献
11.
Thirupaiah Bade 《合成通讯》2013,43(20):2350-2354
The synthesis of 3-(2-(5-(benzylideneamino)-3-phenyl-1H-pyrazol-1-yl)thiazol-4-yl)-4-hydroxy-6-methyl-2H-pyran-2-one derivatives was achieved through a one-pot, four-component reaction involving condensation of 3-(2-bromoacetyl)-4-hydroxy-6-methyl-2H-pyran-2-one, thiosemicarbazide, phenacylcyanaide, and various aryl aldehydes in dry alcohol and few drops of acetic acid under reflux condition. This four-component reaction has some advantages such as ease of handling, good yields, and easy workup. All structures of newly prepared compounds were confirmed by analytical and spectral data. 相似文献
12.
13.
The reaction of 3,6-bis(trimethylsiloxy)pyridazine and its 4,5-dihalogen-substituted derivatives with 2-chlorotetrahydrofuran and 2-chlorotetrahydropyran has given 3-hydroxy-1-(tetrahydrofuranyl- and 3-hydroxy-1-(tetrahydropyranyl)-1,6-dihydropyridazin-6-ones, the structure of which as 1-substituted derivatives has been confirmed by an investigation of their IR spectra. On the basis of a study of ionization constants, the hypothesis has been put forward that these compounds exist in the hydroxy form.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 11, pp. 1545–1547, November, 1973. 相似文献
14.
《合成通讯》2013,43(21):3361-3376
The preparation of 4-hydroxy-1-methyl-3-(5-oxo-4,5-dihydro-1H-3-pyrazolyl)-1,2-dihydro-2-quinolinone (3) and its hydrazono-, aminomethylidene- and arylidene derivatives has been achieved. The synthesis of fused heterocyclic polynuclear systems containing quinolinone moiety is also described. 相似文献
15.
A new series of (4′-hydroxy-3′,5′-dinitrophenyl) (3-aryloxiran-2-yl) methanone derivatives has been synthesized by the reaction of 4′-hydroxy-3′,5′-dinitro-substituted chalcones and alkaline H2O2. The resulted oxiranes on sulfanilic acid-catalyzed aminolysis afforded 2-hydroxy-1-(4′-hydroxy-3′,5′-dinitrophenyl)-3-aryl-3-(arylamino) propan-1-one derivatives. The advantage of this environmentally benign safe protocol offers a simple reaction set-up, mild reaction conditions, high product yields and short reaction time. The catalyst was reused several times without significant loss of catalytic activity. 相似文献
16.
5-(2,5-Dimethylphenyl)-1,2-oxazole-3-carbaldehyde oxime reacted with acetic anhydride in pyridine to give 5-(2,5-dimethylphenyl)-1,2-oxazole-3-carbonitrile which was converted into the corresponding amide oxime by treatment with hydroxylamine. O-Acyl derivatives of N′-hydroxy-5-(2,5-dimethylphenyl)-1,2-oxazole-3-carboximidamide underwent heterocyclization into 5-substituted 3-[5-(2,5-dimethylphenyl)-1,2-oxazol-3-yl]-1,2,4-oxadiazoles on heating in acetic acid. 相似文献
17.
I. V. Ukrainets L. V. Sidorenko O. V. Gorokhova S. V. Slobodzyan 《Chemistry of Heterocyclic Compounds》2007,43(1):63-66
The reaction of 2-ethoxycarbonylmethyl-4H-3,1-benzoxazin-4-one with malononitrile in dry pyridine leads to 1-hydroxy-3,6-dioxo-4,6-dihydro-3H-pyrimido[1,2-a]quinoline-5-carbonitrile.
Acetoacetic and cyanoacetic esters under analogous conditions form anilides of 4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxylic
acid while diethyl malonate gives N,N′-di-2-carboxyanilides of malonic acid.
__________
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 75–79, January, 2007. 相似文献
18.
A. A. Avetisyan I. L. Aleksanyan A. A. Pivazyan 《Chemistry of Heterocyclic Compounds》2005,41(4):471-474
A method has been developed for the synthesis of substituted 4-hydroxy- and 4-amino-2-methyl-3-(2-methylindol-3-yl)methylquinolines by treating the corresponding 4-hydroxy(chloro)-2-methyl-3-(3-oxobutyl)quinolines with phenylhydrazine hydrochloride. It was found that nucleophilic substitution occurred in the case of the 4-chloroquinolines together with subsequent rearrangement to give the 4-amino derivatives. The thiosemicarbazones of the corresponding 4-hydroxy-2-methyl-3-(3-oxobutyl)quinolines were also obtained.__________Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 554–557, April, 2005. 相似文献
19.
V. I. Pavlovsky E. A. Semenishina S. A. Andronati I. G. Filippova Yu. A. Simonov M. Gdaniec J. Lipkowski 《Chemistry of Heterocyclic Compounds》2009,45(11):1379-1387
On interacting 7-bromo-5-(2-chlorophenyl)-3-hydroxy-1,2-dihydro-3H-1,4-benzodiazepin-2-one with methyl, hexyl, dodecyl, and
cetyl tosylates, 1-alkyl-7-bromo-5-(2-chlorophenyl)-1,2,4,5-tetrahydro-3H-1,4-benzodiazepin-2,3-diones, and 1-alkyl-7-bromo-5-(2-chlorophenyl)-3-hydroxy-1,2-dihydro-3H-1,4-benzodiazepin-
2-ones were obtained. Only the dione was formed in the case of hexyl tosylate. On alkylating with methyl tosylate only the
3-hydroxy derivative was formed. It was shown that at pH 14 the 1-cetyl and 1-dodecyl-3-hydroxy derivatives were completely
converted into the corresponding diones. The molecular and crystal structures of the compounds were established by X-ray structural
analysis. 相似文献
20.
Kakehi A Ito S Suga H Miwa T Mori T Fujii T Tanaka N Kobayashi T 《Chemical & pharmaceutical bulletin》2003,51(1):75-84
Various ethyl 1-arylcarbonyl-3-[(un)substituted methylthio]thieno[3,4-b]indolizine-9-carboxylates were synthesized in good yields by a novel methodology in which the S-alkylation of 5-arylcarbonyl-4-ethoxycarbonylmethyl-3-(1-pyridinio)thiophene-2-thiolates with alkyl or benzyl halides, the 1,5-dipolar cyclization of the resulting pyridinium salts in the presence of a base, and the aromatization were performed. In the X-ray analyses of some 3-(benzylthio)thieno[3,4-b]indolizine-9-carboxylates, a gauche and two anti conformers in relation to the exocyclic sulfide linkage were found. Interestingly, all of the 3-(benzylthio)thieno[3,4-b]indolizine derivatives showed significant high-field shifts (delta up to 0.3 ppm) for the 5- and 6-proton signals compared with those of the 3-methylthio derivatives in the (1)H-NMR spectra and exhibited a definite absorption band near 425 nm in their UV spectra, indicating an intramolecular arene-arene interaction between the thieno[3,4-b]indolizine and the phenyl ring. 相似文献