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2.
Essam Kh. Ahmed 《Phosphorus, sulfur, and silicon and the related elements》2013,188(4):989-1000
Ethyl 2-methyl-11-oxo-9, 10-dihydro-1 H , 11 H -pyrido[4",3":4',5']thieno[2',3':4,5]pyrimido[2,1-b][1,3,4]thiadiazine-8(7 H )-carboxylate 7 has been synthesised by the reaction of ethyl 3-amino-4-oxo-2-thioxo-1,3,4,5,6,8-hexahydropyrido[4',3':4,5]thieno[2,3-d]pyrimidine-7(2 H )-carboxylate 2 with allylbromide followed by treatment with bromine and subsequent dehydrobromination of the brominated product 5 with ethanolic sodium hydroxide. Its isomeric ethyl 2-methyl-11-oxo-9,10-dihydro-3 H ,11 H -pyrido[4",3Prime;:4',5']thieno[2',3':4,5]pyrimido[2,1-b][1,3,4]thiadiazine-8(7 H )-carboxylate 8 has been obtained by condensation of 2 with chloroacetone followed by cyclization of the intermediate 9 with p -toulenesulfonic acid. The thiadiazino derivatives 11 , 13 , 15 were prepared through the reaction of 2 with the appropriate f -halocarbonyl compounds followed by cyclization reactions of the intermediates 10 , 12 , 14 . 相似文献
3.
Igor V. Pimkov Archana Nigam Kiran Venna Fraser F. Fleming Pavlo V. Solntsev Victor N. Nemykin Partha Basu 《Journal of heterocyclic chemistry》2013,50(4):879-886
The bicyclic pyran thiolone tetrahydro‐3αH‐[1,3]dithiolo[4,5‐β]pyran‐2‐thione ( 3a ) engages in a highly unusual fragmentation in the presence of DDQ. The pyran thiolone, 3a , was synthesized by chlorination of 3,4‐dihydro‐2H‐pyran ( 1 ) followed by condensing with CS2 and NaSH. Reaction of 3a with DDQ generates the isomerized pyran thiolone tetrahydro‐3αH‐[1,3]dithiolo[4,5‐β]pyran‐2‐thione ( 3b ) and 4‐benzyl‐5‐(3‐hydroxypropyl)‐1,3‐dithiole‐2‐thione ( 4 ) via a deep‐seated rearrangement. The identity of 3b was confirmed by single crystal X‐ray analysis: P21/c, a = 5.807(9) Å, b = 12.99(2) Å, c = 11.445(15), β = 113.23(6)°. Mechanistic experiments and computational insight is used to explain the likely sequence of events in the highly unusual formation of 4 . Collectively, these results establish fundamental reactivity patterns for further research in this area. 相似文献
4.
Henryk Foks Mieczysław Janowiec Zofia Zwolska Ewa Augustynowicz-Kopeć 《Phosphorus, sulfur, and silicon and the related elements》2013,188(12):2519-2526
2,2′-Sulfinyl-bis(4-methyl phenol) 3 and it's thio derivative have been synthesized in this work. The reduction process of sulfoxide 3 to its thio derivative 5 was accomplished in the presence of Zn/AcOH/SiO2, under microwave irradiation. The structures have been confirmed by spectroscopic (IR, 1HNMR, 13CNMR) and single crystal x-ray diffraction methods. 2,2′-Sulfinyl-bis(4-methyl phenol) 3 crystallizes in the space group Cc of the monoclinic system with four molecules in the unit cell of dimensions a = 11.425(2) Å, b = 13.530(2) Å, c = 9.5215(17) Å, β = 117.289(4) Å, and 2,2′-thio-bis(4-methyl phenol) 5 crystallizes in the space group P 212121 of the orthorhombic system with four molecules in the unit cell of dimensions a = 9.021(1) Å, b = 10.523(2) Å, c = 13.607(2) Å, α = 90. The structures have been refined to final values for the crystallographic R factor of 0.0189(3) and 0.0248(5) based on 2999 and 3720 observed independent reflections respectively. 相似文献
5.
Adel A.-H. Abdel-Rahman Amira K. F. Shaban Ibrahim F. Nassar Dina S. EL-Kady Nasser S. M. Ismail Samy F. Mahmoud Hanem M. Awad Wael A. El-Sayed 《Molecules (Basel, Switzerland)》2021,26(13)
New pyridine, pyrazoloyridine, and furopyridine derivatives substituted with naphthyl and thienyl moieties were designed and synthesized starting from 6-(naphthalen-2-yl)-2-oxo-4-(thiophen-2-yl)-1,2-dihydropyridine-3-carbonitrile (1). The chloro, methoxy, cholroacetoxy, imidazolyl, azide, and arylamino derivatives were prepared to obtain the pyridine-−C2 functionalized derivatives. The derived pyrazolpyridine-N-glycosides were synthesized via heterocyclization of the C2-thioxopyridine derivative followed by glycosylation using glucose and galactose. The furopyridine derivative 14 and the tricyclic pyrido[3′,2′:4,5]furo[3,2-d]pyrimidine 15 were prepared via heterocyclization of the ester derivative followed by a reaction with formamide. The newly synthesized compounds were evaluated for their ability to in vitro inhibit the CDK2 enzyme. In addition, the cytotoxicity of the compounds was tested against four different human cancer cell lines (HCT-116, MCF-7, HepG2, and A549). The CDK2/cyclin A2 enzyme inhibitory results revealed that pyridone 1, 2-chloro-6-(naphthalen-2-yl)-4-(thiophen-2-yl)nicotinonitrile (4), 6-(naphthalen-2-yl)-4-(thiophen-2-yl)-1H-pyrazolo[3,4-b]pyridin-3-amine (8), S-(3-cyano-6-(naphthaen-2-yl)-4-(thiophen-2-yl)pyridin-2-yl) 2-chloroethanethioate (11), and ethyl 3-amino-6-(naphthalen-2-yl)-4-(thiophen-2-yl)furo[2,3-b]pyridine-2-carboxylate (14) are among the most active inhibitors with IC50 values of 0.57, 0.24, 0.65, 0.50, and 0.93 µM, respectively, compared to roscovitine (IC50 0.394 μM). Most compounds showed significant inhibition on different human cancer cell lines (HCT-116, MCF-7, HepG2, and A549) with IC50 ranges of 31.3–49.0, 19.3–55.5, 22.7–44.8, and 36.8–70.7 μM, respectively compared to doxorubicin (IC50 40.0, 64.8, 24.7 and 58.1 µM, respectively). Furthermore, a molecular docking study suggests that most of the target compounds have a similar binding mode as a reference compound in the active site of the CDK2 enzyme. The structural requirements controlling the CDK2 inhibitory activity were determined through the generation of a statistically significant 2D-QSAR model. 相似文献
6.
Gameel A. M. El-Hag Ali 《Phosphorus, sulfur, and silicon and the related elements》2013,188(4):711-720
A variety of new thiazolo[3,2- a ]pyridine derivatives 2a-h having 3-indolyl group were produced by refluxing 1a with different benzylidenemalononitrile derivatives. Reactivity of compound 4 toward some nitrogen nuclcophiles was investigated. Thus, the novel pyrazoles 6a , b were obtained when compound 4 was allowed to react with hydrazine and phenyl hydrazine in ethanol under reflux. On the other hand, pyrazolo[3',4':4,5]thiazolo[3,2- a ]-3-aza[1,8]naphthyridine 8 was formed by condensation of compound 4 with benzoyl hydrazine. Finally, condensed heterocyclic compounds containing pyran rings 9 and 10 were obtained by treatment compound 4 with active ethylene compounds. 相似文献
7.
Cornelis M. Moorhoff 《Monatshefte für Chemie / Chemical Monthly》2003,134(1):61-67
Summary. Wittig condensations of α,β-unsaturated carbonyl compounds with ethyl 3-ethoxy-4-(triphenylphosphoranylidene)-2-butenoate gave good
to high yields of (2E,4E,6E)-ethyl 3-ethoxy-2,4,6-alkatrienoates. Some of last mentioned compounds were almost quatitatively hydrolysed to (4E,6E)-ethyl 3-oxo-4,6-alkadienoates. This method can therefore be used as an attractive alternative for the preparation of unsaturated
conjugated β-keto esters previously prepared in very low yields from α,β-unsaturated carbonyl compounds and ethyl 3-oxo-4-(triphenylphosphoranylidene)butanoate.
Present address: Boron Molecular Pty. Ltd., PO Box 756, Noble Park, VIC 3174, Australia. E-mail: cmoorhoff@boronmolecular.com
Received June 17, 2002; accepted June 21, 2002 相似文献
8.
The Knoevenagel condensations of 5-[3-(trifluoromethyl)phenyl]furan-2-carbaldehyde with seven compounds containing an active
methyl or methylene group have been studied. The compounds used were: methyl 2-cyanoacetate, malononitrile, 2-furylacetonitrile,
acetophenone, 2-thioxo-1,3-thiazolidin-4-one (rhodanine), 5,5-dimethylcyclohexane-1,3-dione (dimedone), and methyl 2-azidoacetate.
The effect of microwave irradiation on the condensation reactions was studied and compared with “’classical”’ conditions.
Thermolysis of methyl 2-azido-3-{5-[3-(trifluoromethyl)phenyl]-2-furyl}propenoate afforded methyl 2-[3-(trifluoromethyl)phenyl)]-4H-furo[3,2-b]pyrrole-5-carboxylate.
(2E)-3-{ 5-[3-(Trifluoromethyl)phenyl]-2-furyl}propenoic acid was converted to the corresponding azide, which was cyclized
on heating into 2-[3-(trifluoromethyl)phenyl)]-4,5-dihydrofuro[3,2-c]pyridin-4-one. The latter after successive action of
POCl3 and NH2NH2-Pd/C gave 2-[3-(trifluoromethyl)-phenyl]furo[3,2-c]pyridine.
Published in Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 825–831, June, 2006. 相似文献
9.
A convenient,effcient and environmentally benign procedure has been developed for the synthesis of pyrano[4,3-b]pyran derivatives via a one-pot,three-component reaction of 4-hydroxy-6-methylpyran-2-one,aldehydes and malononitrile in water using H6P2W18O62á18H2O as catalyst.Reusability of the catalyst and reaction media,short reaction times and easy isolation of products are some added advantages of the present methodology. 相似文献
10.
Z. Stec 《Monatshefte für Chemie / Chemical Monthly》1993,124(3):331-332
Summary 2-Acetoxy- and 2-Hydroxy-2,3-dihydronaphtho[1,8-bc]pyranes were synthesized by decomposition of 1-hydroperoxy-1,2-dihydroacenaphthylene in acetic acid in the presence of perchloric acid.
Synthese von 2-Acetoxy- und 2-Hydroxy-2,3-dihydronaphtho[1,8-bc]pyran
Zusammenfassung 2-Acetoxy- und 2-Hydroxy-2,3-dihydronaphtho[1,8-bc]pyrane konnten durch Zersetzung von 1-Hydroperoxy-1,2-dihydroacenaphthylen in Essigsäure in Anwesenheit von Perchlorsäure synthetisiert werden.相似文献
11.
吡喃并[4,3-b]吡喃衍生物与牛血清白蛋白作用的荧光光谱 总被引:1,自引:0,他引:1
用荧光光谱法分析了在生理条件下一种吡喃并[4,3-b]吡喃衍生物—2-氨基-7-甲基-4-(4-硝基苯)-5-氧代-4H,5H-吡喃并[4,3-b]吡喃-3-腈与牛血清白蛋白的作用机制。求得不同温度下二者的结合常数和结合位点数,探讨了微量金属离子对实验体系结合常数的影响,并根据热力学参数确定了这种吡喃并[4,3-b]吡喃衍生物与牛血清白蛋白之间的作用力类型。根据Frster非辐射能量转移机理,测定了这种吡喃并[4,3-b]吡喃衍生物与牛血清白蛋白相互结合时,能量给体-受体间的作用距离和能量转移效率,并用同步和三维荧光技术讨论了其衍生物对牛血清白蛋白构象的影响。结果表明,吡喃并[4,3-b]吡喃衍生物主要以静态猝灭方式使牛血清白蛋白荧光强度显著降低,二者主要凭借氢键和范德华力结合。 相似文献
12.
H. M. Moustafa A. Khodairy H. Abdel-Ghany 《Phosphorus, sulfur, and silicon and the related elements》2013,188(8):1689-1701
3,4-Diamino-2,5-dicarbethoxythieno[2,3-b]thiophene ( 1 ) was allowed to react with NaNO 2 and active methylenes to afford the corresponding azo compounds 2a-c . Hydrazonyl chloride 2a was treated with carbon disulfide, phenyl isothiocyanate, benzonitrile, benzyl cyanide, malononitrile, benzalaniline, ethyl mercaptoacetate, and ethyl glycinate to give 1,3,4-thiadiazolyl-, s-triazolyl-, 1,3,4-thiadiazinyl-, 1,3,4-triazinylthieno[2,3-b]thiophenes 3-6 respectively. The reaction of 2b,c with urea, thiourea, and guanidine afforded pyrimidinyl- and thiazinylazothieno [2,3-b]thiophenes 7-10 respectively. Bithiazolylthieno[2,3-b]thiophenes 11 and 13 were synthesized by treating compound 1 with CS 2 along with halo compounds. The addition of S,S-, N,S-, and N,O-acetals to the Schiff base 14 afforded compounds 15-17 respectively. 相似文献
13.
A. Deeb A. Essawy A. M. El-Gendy A. Shaban 《Monatshefte für Chemie / Chemical Monthly》1990,121(4):281-287
Summary 3-Carbethoxy-4,6-diphenyl-2-pyrridine sulfonamide (5), can be cyclized to 3-oxo-2,3-dihydro-4,6-diphenylisothiazolo[5,4-b]pyridine-1,1-dioxide (2). Oxidation of pyridinethione6 with Cl2/H2O gave the sulfonyl chloride derivative7, which can be ammonolyzed to 3-amino-4,6-diphenylisothiazolo[5,4-b]pyridine-1,1-dioxide (8), and 3-cyano-4,6-diphenylpyridine-2-sulfonamide (9). Hydrolysis of6 gave 3-carboxamido-2(1H)pyridinethione (12) which can be oxidized with iodine to 3-oxo-4,6-diphenyl-2,3-dihydroisothiazolo[5,4-b]pyridine (13). 3-Methyl-4,6-diphenylisothiazolo[5,4-b]pyridine-1,1-dioxide (17) was also prepared from6.
Heterocyclensynthese mit 3-Cyano-2(1H)pyridinthion: Synthese von 3-Oxo-2,3-dihydroisothiazolo-[5,4-b]pyridin und verwandten Verbindungen
Zusammenfassung 3-Carbethoxy-4,6-diphenyl-2-pyridinsulfonamid (5) kann zu 3-Oxo-2,3-dihydro-4,6-diphenylisothiazolo[5,4-b]pyridin-1,1-dioxid (2) cyclisiert werden. Die Oxidation des Pyridinthions6 mit Cl2/H2O ergab das Sulfonylchlorid-Derivat7, das mit Ammoniak zu 3-Amino-4,6-diphenylisothiazolo[5,4-b]pyridin-1,1-dioxid (8) und 3-Cyano-4,6-diphenylpyridin-2-sulfonamid (9) umgesetzt werden kann. Die Hydrolyse von6 ergab 3-Carboxamido-2(1H)pyridinthion (12), das mit Jod zu 3-Oxo-4,6-diphenyl-2,3-dihydroisothiazolo[5,4-b]pyridin (13) oxidiert wurde. 3-Methyl-4,6-diphenyl-isothiazolo[5,4-b]pyridin-1,1-dioxid (17) wurde ebenfalls aus6 hergestellt.相似文献
14.
Mohamed A. A. Elneairy Mohamed A. M. Gad-Elkareem Azza M. Abdel-Fattah 《Phosphorus, sulfur, and silicon and the related elements》2013,188(6):1451-1466
Pyrdine-2(1H)-thione 1 reacted with ethyl chloroacetate 2 to give 2-S-ethoxy-carbonylmethylpyridine derivative 3, which could be cyclized into thieno[2,3-b]-pyridine-2-carbohydrazide derivative 5 by boiling with hydrazine hydrate. The latter compound reacted with cinnamonitrile derivatives 6a, b, triethylorthoformate, formic acid, dimethylformamide-dimethylacetal, and diethyl carbonate to give the corresponding shiff base 7a, b and pyrido[3′,2′;-4,5]thieno[3,2-d]pyrimidine derivatives 10–13 in respective manner. On the other hand, compound 5 also reacted with carbondisulphide and phenyl isothiocyanate to afford the corresponding 2-(1,3,4-oxadiazolo-2-yl)thieno[2,3-b]pyridine derivatives 18 and 22. Finally, compound 5 reacted with some β-dicarbonyl compounds, such as ethyl acetoacetate, acetylacetone and ethyl β-arylazoacetoacetate, to yield the corresponding 2-(pyrazol-1-yl-carbonyl)thieno[2,3-b]pyridine derivatives 24, 25, and 27 respectively. 相似文献
15.
Synthesis and Crystal Structure of the Adducts [DB-18C6] · CH3CN · CH3CSOH and [DC-18C6](CH3CSOH)2 as well as of the Salt-like Compounds [Cs(B-15C5)2]CH3CSS and [Cs(DB-18C6)]2S5(DMF)21) The reaction products of crown ethers, cesium, and sulfur in aprotic solvents like acetonitrile and dimethylformamide strongly depend on the reaction conditions. Using CH3CN as a solvent, sometimes neutral host-guest adducts crystallize only, e.g., [dibenzo-18C6] · CH3CN · CH3CSOH (monoclinic, S. G. P21/c, Z = 4, a = 9.73(1) Å, b = 22.03(1) Å, c = 11.86(1) Å, β = 91.8(1)°) or [dicyclohexyl-18C6](CH3CSOH)2 (monoclinic, S. G. P21/n, Z = 2, a = 7.75(1) Å, b = 10.32(1) Å, c = 17.73(1) Å, β = 95.7(1)°). The monothioacetic acid, CH3CSOH, must be regarded as the first product of the hydrolysis of CH3CN. Furthermore, another product of this kind of hydrolysis, CH3CSSH, is obtained too. Therefore, we also obtain the salt-like compound [Cs(benzo-15C5)2]CH3CSS (monoclinic, S. G. C2/c, Z = 4, a = 16.05(1) Å, b = 16.73(1) Å, c = 13.11(1) Å, β = 106.3(1)°). If the solvent DMF is used, the pentasulfide [Cs(dibenzo-18C6)]2S5(DMF)2 crystallizes (monoclinic, S. G. P21/n, Z = 4, a = 14.79(1) Å, b = 14.24(1) Å, c = 25.74(1) Å, β = 92.7(1°. The S52? anions show the cis-conformation. 相似文献
16.
The novel title compound(Z)-N-(4-bromo-5-ethoxy-3,5-dimethylfuran-2(5H)-yli-dene)-4-methylbenzenesulfonamide 1(C15H18BrNO4S) has been unexpectedly synthesized by the aminohalogenation reaction of ethyl 2-methylpenta-2,3-dienoate with TsNBr2,and characterized by mp,IR,1H NMR,EIMS,ESIHRMS and single-crystal X-ray diffraction.It crystallizes in mono-clinic,space group P21/c with a = 11.714(5),b = 14.106(5),c = 10.402(4) ,β = 97.298(8)°,V = 1704.9(12) 3,Mr = 388.27,Z = 4,Dc = 1.513 g/cm3,μ(MoKα) = 2.549 mm-1,F(000) = 792,the final R = 0.033 and wR = 0.062 for 3098 observed reflections(Ⅰ 2σ(Ⅰ)). 相似文献
17.
18.
Mehmet Somer Wilder Carrillo-Cabrera Eva Maria Peters Karl Peters Hans Georg von Schnering 《无机化学与普通化学杂志》1998,624(11):1915-1921
Tetrarubidiumnonagermanid(4–)-ethylendiamin, Rb4[Ge9][en] Orange-farbene Kristalle von Rb4[Ge9][en] erhält man nach der Austauschreaktion einer Lösung von ,NaGe2.25‘ (precursor) in Ethylendiamin (en) mit festem RbI bei 360 K und nachfolgender langsamer Abkühlung. Die Verbindung ist äußerst empfindlich gegen Oxidation und Hydrolyse. Der thermische Abbau im dynamischen Vakuum beginnt mit der vollständigen Abgabe von en bei 350 K. Es folgt die Sublimation von Rubidium in vier weiteren Stufen (Rb8Ge25, Rb8Ge44, RbxGe136 mit x È 16, Ge). Das Ramanspektrum zeigt die charakteristischen Banden des Anions [Ge9]4– bei 151, 163, 185 und 222 cm–1. Rb4[Ge9][en] kristallisiert in einem neuen Strukturtyp (Raumgruppe P21/m; a = 15.353 Å, b = 16.434 Å, c = 15.539 Å, β = 113.75°; Z = 6; Pearsonsymbol mP198-40), der als hierarchische Variante der Strukturen von Al4YbMo2 und CrB4 (hierarchische Basistypen, „initiators”︁) beschrieben werden kann, indem Atome partiell durch Aggregate ersetzt werden: B4[□][Cr] ≙ Al4[Yb][Mo]2 ≙ Rb4[Ge9][en]1–2. Drei kristallographisch unabhängige [Ge9]4–-Cluster sind in ein vierbindiges 465-Netz aus Rb-Atomen eingebettet, ein Netzwerk kondensierter Tetraasterane. Die Cluster sind verzerrte überkappte tetragonale Antiprismen mit D1(Ge–Ge) = 2.57 Å (16 Ç ) und D2(Ge–Ge) = 2.84 Å (4 Ç ). Die Atome der Cluster mit D1 und D2 liegen auf der Oberfläche eines Rotationsellipsoids (a = b = 2.136 Å, c = 2.431 Å). Die en-Moleküle befinden sich in offenen Kanälen entlang [1¯ 0 1]. Die Koordinationen [Ge9]Rb12/4 und Rb [Ge9]4/12 en2/8 zeigen, daß beim ersten Schritt der Solvatisierung Kationen und Clusteranionen nicht voneinander getrennt werden. 相似文献
19.
Mohamed A. M. Gad-Elkareem Azza M. Abdel-Fattah Mohamed A. A. Elneairy 《Phosphorus, sulfur, and silicon and the related elements》2013,188(4):891-911
Nicotinic acid esters 3a–c were prepared by the reaction of pyridine-2(1H)-thione derivative 1 with α-halo-reagents 2a–c. Compounds 3a–c underwent cyclization to the corresponding thieno[2, 3-b]pyridines 4a–c via boiling in ethanol/piperidine solution. Compounds 4a–c condensed with dimethylformamide-dimethylacetal (DMF-DMA) to afford 3-{[(N,N-dimethylamino)methylene]amino}thieno[2, 3-b]- pyridine derivatives 6a–c. Moreover, compounds 4a–c and 6a–c reacted with different reagents and afforded the pyrido[3′,2′:4, 5]thieno[3, 2-d]pyrimidine derivatives 10a–d, 11a–c, 12a,b, 14a,b, 17, and 19. In addition, pyrazolo[3, 4-b]pyridine derivative 20 (formed via the reaction of 1 with hydrazine hydrate) reacted with ethylisothiocyanate yielded the thiourea derivative 21. Compound 21 reacted with α-halocarbonyl compounds to give the 3-[(3H-thiazol-2-ylidene)amino]-1H-pyrazolo[3, 4-b]pyridine derivatives 23a–c, 25, and 27a,b. 相似文献
20.
Synthesis and Structure of 2-Isobutyl-6-(2'''',4''''-dichlorophenyl)imidazo[2,1-b]-1,3,4-thiadiazole 总被引:1,自引:0,他引:1
1INTRODUCTIONThethiadiazoleandimidazolecompoundsareextensivelystudiedduetotheirspectrumbioacti-vities[1~4].Amongthem,theimidazo[2,1-b]-1,3,4-thiadiazolederivativesarepharmaceuticallyimpor-tantbecauseoftheirimmunostimulant[5],antifugal[6],antimicrobial[7]… 相似文献