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1.
Abdel‐Zaher Abdel‐Aziz Elassar 《中国化学会会志》2006,53(4):901-907
Methylquinoxaline derivative 1 undergoes bromination to give bromomethyl quinoxaline 2 , which could be transferred to cyanomethyl quinoxaline 3 . The latter compound 3 readily coupled with arene diazonium salts to give hydrazone derivatives 5a‐c . Compounds 5a,b reacted with active methylene reagents to give the target ring system, quinoxalinylpyridazine derivatives 8a‐c . Compound 1 reacted with DMFDMA to give the enamine derivative 9 , which coupled with arene diazonium salts to give the aldehydic hydrazone derivatives 10a‐c . Compound 10 reacted with active methylene compounds to give quinoxalinylpyridazine derivatives. UV characterization of some of the prepared compounds was reported. 相似文献
2.
《Arabian Journal of Chemistry》2014,7(5):775-780
3-Amino-5-phenyl-2-ethoxycarbonylthieno[2,3-c]pyridazine (6) was prepared by reaction of 4-cyano-6-phenylpyridazine-3(2H)-thione (4) with ethyl chloroacetate in the presence of sodium ethoxide. Hydrazinolysis of compound 6 yielded the corresponding carbohydrazide, (9) which on treatment with acetylacetone and ethyl acetoacetate produced the novel thieno[2,3-c]pyridazines (10 and 11). Treatment of compound 9 with nitrous acid yielded the corresponding carboazide (13), which upon boiling in toluene furnished imidazo[4′,5′:4,5]thieno[2,3-c]pyridazine (15). Pyrimidothienopyridazines (16–18) were achieved by cyclocondensation of compound 9 with some reagents, namely acetic anhydride, formic acid, and triethyl orthoformate. The newly synthesized compounds were confirmed by elemental analyses and spectral data. The antibacterial activities of the new compounds were also evaluated. 相似文献
3.
An efficient and straightforward method for the preparation of spirodiazine derivatives is reported which involves mild reaction conditions and easily accessible reactants. A new class of spiroazaheterocycles, spiro[pyrrolidine-pyrrolo[3,4-c]pyrroles], is obtained. A feasible explanation is given for the unexpected results obtained at high energy (high temperatures, MW and ultrasound irradiation). 相似文献
4.
Xiu-rong Li Zhi-hui Zhang Xiu-feng Liu Hong Gao Xiang-nan Zhang Zhi-jin Fan 《Journal of chemical crystallography》2008,38(10):781-786
Abstract Two new complexes, [Cu(L)2(CH3OH)] · (ClO4)2 (1) and [Cu(L)2(H2O)] · (NO3)2 (2), have been synthesized and their crystal structures have been determined by X-ray analysis, where L = 3-(3,5-bimethylpyrazole-yl)-6-chloro-pyridazine].
The complex 1 crystallizes in the monoclinic, space group C2/c, and the coordination configuration of copper (II) is better described as trigonal pyramidal geometry with four N atoms from
L and one Omethanol. The coordination configuration of 2 is quite similar to that of 1 except Owater instead of Omethanol. The intermolecular hydrogen bonds link the repeat units and extend the molecules to multinuclear structures in both compounds.
The spectral properties of the title compounds have been studied and discussed. Furthermore, the antibacterial activities
of the title compounds have been detected, the results indicate that the ligands and two copper(II) complexes exhibit certain
fungicidal activities again several bacteria.
Index Abstract Two new complexes, [Cu(L)2(CH3OH)]·(ClO4)2 (1) and [Cu(L)2(H2O)]·(NO3)2 (2), have been synthesized and their crystal structures
have been determined by X-ray analysis, where L= 3-(3,5-bimethylpyrazole-yl)-6-chloro-pyridazine. The intermolecular hydrogen
bonds extend the molecules to multinuclear structures in both compounds.
相似文献
5.
The landscape of organic molecule on Si(100) surface has a great significance for organic functionalisation of Si semiconductor. Several possible adsorption configurations for pyridazine on Si(100) surface have been forecasted by systemic comparison and investigation. The C1s XPS and NEXAFS spectra of these adsorption systems based on density functional theory and full core-hole potential approximation have been calculated. Although the sensibility of XPS to these adsorption configurations is not very strong, these configurations can be absolutely distinguished by NEXAFS spectra, which will bring tremendous reference to the future experimental study. Mode II, III, V and VI have a significantly higher adsorption energy, which are most likely to be present in experiment. In addition, we have made the research on specific sources of the peaks in spectra by analysing their decomposed NEXAFS spectra, the results show that the Carbon atoms which do not bond to surface atoms, make the most contribute to the intensity of characteristic peaks in spectra. 相似文献
6.
The 2‐ethoxy carbonyl methylene thiazol‐4‐one ( 3 ) reacts with acetophenone ( 4 ) to give the ethyl 2‐(4‐oxo‐4,5‐dihydro‐thiazol‐2‐yl)‐3‐phenyl‐2‐butenoate ( 5 ). The reactivity of the latter product towards aromatic aldehydes 6a‐d , cyanomethylene reagents 9a,b , aromatic aldehydes 13a‐d , phenylisothiocyanate ( 16 ), elemental sulfur and aromatic amines ( 20a‐c ) was studied to give arylidene, pyridine, thiophene and anilide derivatives. Some of the newly synthesized derivatives were used to synthesize fused derivatives. The antimicrobial activities of the newly synthesized products were tested in vitro for antimicrobial activity against two bacterial isolates, one saprophytic (Escherichia coli) and the other parasitic (Xanthomonas citri) and for antifungal activity against one saprophytic (Aspergillus fumigatus) and two phytopathogenics (Rhizoctonia solani and Fusarium oxysporum). 相似文献
7.
The hydrogen bond structure and interaction energy on the ground state of pyridazine and water complex are studied with B3LYP and MP2 method. All calculations show that there are strong interactions for a hydrogen bond N…H-O and large red-shifts for the symmetric H-O stretching vibrational frequencies in the pyridazine and water complex. The first singlet 1(n, π ) and 1(π,π) vertical excitations of the monomer pyridazine and the hydrogen bond between a pyridazine molecule and a water molecule have been investigated with time-dependent density functional theory TDB3LYP method. 相似文献
8.
Uday Joshi Muriel Pipelier Jean-Paul Pradère Stéphanie Legoupy Didier Dubreuil 《Tetrahedron letters》2004,45(5):1031-1033
Pyridazine C-nucleosides have been synthesized by [4+2] cycloaddition of alkynyl C-nucleosides with substituted tetrazines. These pyridazines on extrusion of a nitrogen atom afforded novel pyrrole C-nucleosides with good yields. The results of electrochemical and chemical reduction are compared. 相似文献
9.
Vaporization enthalpies for the isomeric diazines were discussed within the context of recent measurements and estimation
techniques. It is suggested that pyridazine shows enigmatic behavior.
相似文献
Joel F. Liebman (Corresponding author)Email: |
10.
Kota Thirumala Prasad A.K. Chandra Kollipara Mohan Rao 《Journal of organometallic chemistry》2010,695(5):707-2022
Reactions of 3,6-bis(2-pyridyl)-4-phenylpyridazine (Lph) with [(η6-arene)Ru(μ-Cl)Cl]2 (arene = C6H6, p-iPrC6H4Me and C6Me6), [(η5-C5Me5)M(μ-Cl)Cl]2, (M = Rh and Ir) and [(η5-Cp)Ru(PPh3)2Cl] (Cp = C5H5, C5Me5 and C9H7) afford mononuclear complexes of the type [(η6-arene)Ru(Lph)Cl]PF6, [(η5-C5Me5)M(Lph)Cl]PF6 and [(Cp)Ru(Lph)(PPh3)]PF6 with different structural motifs depending on the π-acidity of the ligand, electronic properties of the central metal atom and nature of the co-ligands. Complexes [(η6-C6H6)Ru(Lph)Cl]PF61, [(η6-p-iPrC6H4Me)Ru(Lph)Cl]PF62, [(η5-C5Me5)Ir(Lph)Cl]PF65, [(η5-Cp)Ru(PPh3)(Lph)]PF6, (Cp = C5H5, 6; C5Me5, 7; C9H7, 8) show the type-A binding mode (see text), while complexes [(η6-C6Me6)Ru(Lph)Cl]PF63 and [(η5-C5Me5)Rh(Lph)Cl]PF64 show the type-B binding mode (see text). These differences reflect the more electron-rich character of the [(η6-C6Me6)Ru(μ-Cl)Cl]2 and [(η5-C5Me5)Rh(μ-Cl)Cl]2 complexes compared to the other starting precursor complexes. Binding modes of the ligand Lph are determined by 1H NMR spectroscopy, single-crystal X-ray analysis as well as evidence obtained from the solid-state structures and corroborated by density functional theory calculations. From the systems studied here, it is concluded that the electron density on the central metal atom of these complexes plays an important role in deciding the ligand binding sites. 相似文献