Search results for "Oxazole"

showing 10 items of 227 documents

Antibakterielle Wirkstoffe, 6. Mitt.1) 2,4-Unsymmetrisch dialkylierte Pyrimido[1,2-a]benzimidazole

1982

Durch Kondensation von 2-Aminobenzimidazol (1) mit 2,4-Hexandion (2a) entsteht das Isomerenpaar 3a/3b, mit 6-Methyl-2,4-heptandion (2b) das Isomerengemisch 3c/3d, wahrend mit 1-Phenyl-2,4-pentandion (2c) die Isomere 3e und 3f gebildet werden. Die Trennung der Isomere ist durch Saulenchromatographie, die Strukturfestlegung auf spektroskopischem Wege, moglich. 2-Imino-2H-s-triazino[2,1-b]benzoxazol weist antibakterielle Wirksamkeit auf. Antibacterial Drugs, VI: 2,4-Unsymmetrically Dialkylated Pyrimido[1,2-α]benzimidazoles Condensation of 2-aminobenzimidazole (1) with 2,4-hexanedione (2a) leads to the pair of isomers 3a/3b. Condensation with 6-methyl-2,4-heptanedione (2b) yields the isomers 3c…

chemistry.chemical_compoundColumn chromatographychemistryStereochemistryDrug DiscoveryCondensationPharmaceutical ScienceBenzoxazoleAntibacterial activityMedicinal chemistryArchiv der Pharmazie
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Studies in organic mass spectrometry. IV. Electron impact induced fragmentation of 2-substituted 3-(5-isoxazolyl)-4(3H)-quinazolinones of pharmaceuti…

1984

The fragmentation under electron impact of thirteen 2-substituted-3-(5-isoxazolyl)-4(3H)-quinazolinones has been investigated with the aid of metastable ion detection and high resolution measurements. Molecular ions are always abundant and the main primary fragmentation route involves acetonitrile elimination through isoxazole ring opening. The other common processes, particularly those leading to the abundant [R-C8H4N2]+ ion (b or b'), as well as those due to the nature of the 2-substituent are reported and discussed.

chemistry.chemical_compoundFragmentation (mass spectrometry)Bicyclic moleculechemistryOrganic ChemistryMass spectrumOrganic chemistryIsoxazoleMass spectrometryAcetonitrileMedicinal chemistryElectron ionizationIonJournal of Heterocyclic Chemistry
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4-[3-(4-Fluorophenyl)-5-isopropylisoxazol-4-yl]pyridine

2006

The mol­ecular structure of the title compound, C17H15FN2O, was determined in the course of our studies on mitogen-activated protein kinase inhibitors. The exocyclic bond angles at the carbon atoms of the isoxazole ring bearing the pyridyl and 4-fluoro­phenyl rings are 130.0 (2) and 129.2 (2)°, respectively. The pyridine and 4-fluoro­phenyl rings are twisted relative to the isoxazole ring by 80.2 (2) and 19.1 (1)°, respectively.

chemistry.chemical_compoundMolecular geometryChemistryPyridineGeneral Materials ScienceGeneral ChemistryIsoxazoleCondensed Matter PhysicsRing (chemistry)Medicinal chemistryActa Crystallographica Section E Structure Reports Online
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4-[5-(4-Fluorophenyl)-3-isopropylisoxazol-4-yl]pyridine

2006

In the title compound, C17H15FN2O, the exocyclic bond angles at the C atoms of the isoxazole ring bearing the pyridyl and 4-fluoro­phenyl substituents are 129.66 (17) and 134.58 (16)°, respectively. The structure was determined in a study of the mol­ecular geometry of isoxazole derivatives with biological activity as MAPK inhibitors.

chemistry.chemical_compoundMolecular geometryMAPK InhibitorschemistryStereochemistryPyridineGeneral Materials ScienceBiological activityGeneral ChemistryIsoxazoleCondensed Matter PhysicsRing (chemistry)IsopropylActa Crystallographica Section E Structure Reports Online
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A Photochemical One-Pot Three-Component Synthesis of Tetrasubstituted Imidazoles

2014

Tetrasubstituted imidazoles can be formed in a photochemical one-pot synthesis from aldehydes, α-aminonitriles, and isoxazoles. Condensation of the first two components produces α-(alkylideneamino)nitriles which react under basic conditions with the acylazirines formed in situ by photochemical ring transformation of the isoxazole component. This process includes an unusual cleavage of the C(2)-C(3) bond of the acylazirine. The reaction mechanism was studied by DFT calculations.

chemistry.chemical_compoundReaction mechanismchemistryComponent (thermodynamics)Organic ChemistryCondensationPhysical and Theoretical ChemistryIsoxazoleCleavage (embryo)Ring (chemistry)PhotochemistryBiochemistryOrganic Letters
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ChemInform Abstract: Unique Regioselectivity in the C(sp3)-H α-Alkylation of Amines: The Benzoxazole Moiety as a Removable Directing Group.

2015

The benzoxazol-2-yl substituent is easily introduced by oxidative coupling or nucleophilic substitution and can be removed by hydroxide or by hydride reduction.

chemistry.chemical_compoundchemistryHydrideSubstituentNucleophilic substitutionRegioselectivityHydroxideMoietyGeneral MedicineAlkylationBenzoxazoleMedicinal chemistryChemInform
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ChemInform Abstract: On the Reactivity of Nitrosoimidazoles with Acids (the Cusmano-Ruccia Reaction): A Continuous Source of New Ring-into-Ring Inter…

2014

Abstract An extension of the ‘Cusmano–Ruccia’ reaction is reported. 6-(4-chlorophenyl)-3-methyl-5-nitrosoimidazo[2,1- b ]oxazole by the action of hydrochloric acid gives 3-(4-chlorobenzoyl)-5-methyl-1,2,4-oxadiazole ( 13 ); presumably via ammonium ion, CO 2 and methanol elimination. The relevance of the nature of the atom of the B -ring linked to C-2 of the imidazole for the occurrence of the ring-into-ring interconversion has been once more confirmed.

chemistry.chemical_compoundchemistryStereochemistryImidazoleReactivity (chemistry)AmmoniumHydrochloric acidGeneral MedicineMethanolRing (chemistry)IonOxazoleChemInform
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Crystal structure of 5-(4-tert-butoxyphenyl)-3-(4-n-octyloxyphenyl)-4,5-dihydroisoxazole

2019

The molecule of the title compound, C27H37NO3, was prepared by [3 + 2] 1,3-dipolar cycloaddition of 4-n-octylphenylnitrile oxide and 4-tert-butoxystyrene, the latter compound being a very useful intermediate to the synthesis of liquid-crystalline materials. In the molecule, the benzene rings of the n-octyloxyphenyl and tert-butoxyphenyl groups form dihedral angles of 2.83 (7) and 85.49 (3)°, respectively, with the mean plane of the isoxazoline ring. In the crystal, molecules are linked by weak C—H...O hydrogen interactions into chains running parallel to the b axis.

crystal structureCrystallographyOxideGeneral ChemistryCrystal structureisoxazolinesDihedral angleCondensed Matter PhysicsRing (chemistry)Medicinal chemistrysingle crystalsCrystalchemistry.chemical_compoundliquid crystalschemistryLiquid crystalQD901-999General Materials ScienceIsoxazoleBenzene[3 + 2] cycloadditionActa Crystallographica Section E: Crystallographic Communications
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Crystal structure and Hirshfeld surface analysis of 2-[(1,3-benzoxazol-2-yl)sulfanyl]-N-(2-methoxyphenyl)acetamide

2019

Akkurt, Mehmet/0000-0003-2421-0929; Saylam, Merve/0000-0002-7602-4565

crystal structureHydrogen bondGeneral ChemistryCrystal structureDihedral angleCondensed Matter::Mesoscopic Systems and Quantum Hall Effecthydrogen bonding010402 general chemistry010403 inorganic & nuclear chemistryCondensed Matter PhysicsRing (chemistry)01 natural sciences13-benzoxazole ring system0104 chemical scienceslcsh:ChemistryCrystaldimerschemistry.chemical_compoundCrystallographylcsh:QD1-999chemistryHirshfeld surface analysisGeneral Materials ScienceBenzeneAcetamideActa Crystallographica Section E Crystallographic Communications
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Crystal structure of 4-(4-meth-oxy-phen-yl)-4',4'-dimethyl-3-p-tolyl-3',4'-di-hydro-1'H,3H-spiro-[isoxazole-5,2'-naphthalen]-1'-one.

2015

In the title compound, C28H27NO3, the cyclohexanone and isoxazole rings have envelope conformations, with the methylene and spiro C atoms as the flaps, respectively. The mean plane of the isoxazole ring is inclined slightly to thep-tolyl ring, making a dihedral angle of 14.20 (9)°, and is nearly perpendicular to the mean plane through the tetralone moiety and to the methoxyphenyl ring [dihedral angles = 83.41 (8) and 72.12 (9)°, respectively]. The crystal packing is stabilized mainly by van der Waals forces.

crystal structureisoxazoleGeneral ChemistryCrystal structureDihedral angleCondensed Matter PhysicsRing (chemistry)Data Reportstetra­loneCrystallcsh:ChemistryCrystallographychemistry.chemical_compoundsymbols.namesaketetralonechemistrylcsh:QD1-999TetralonesymbolsMoietyGeneral Materials ScienceIsoxazolevan der Waals forceActa crystallographica. Section E, Crystallographic communications
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