Search results for "Oxamide"

Muskelrelaxantien, 4. Mitt. Monoacylbutyroguanamine

1986

Die Umsetzung von Butyroguanamin (1) mit den Carbonsaureanhydriden 2a−f bei 80–120° fuhrt zu den Monoacylbutyroguanaminen 3a−f, deren Struktur durch IR-, 1H-NMR- und MS-Spektren untermauert wird. Unter den hier beschriebenen Verbindungen weisen insbesondere 3e muskelrelaxierende und antidiabetische und 3a trichomonazide und antivirale Wirksamkeit auf, wahrend mit 3b−d herbizide Wirkungen beobachtet werden. Muscle Relaxants, IV: Monoacylbutyroguanamines Reaction of butyroguanamine (1) with the carboxylic acid anhydrides 2a−f at 80–120°C leads to the monoacylbutyroguanamines 3a−f, the structure of which is supported by IR, 1H-NMR, and mass spectra. Among the compounds described here, particul…

Massenspektrometrische Untersuchungen an Edukten für die Synthese H2-aktiver Substanzen

1982

Unter den Bedingungen der Elektronenstosionisation wurden 4-[(2-Aminoethoxy)-methyl]-5-methyl-imidazo (1), die Imidazolderivate mit N-substituierter Ethylendiamin-Struktur 2–5 sowie die Imidazolcarboxamide 6–8 massenspektrometrisch untersucht. Der Mechanismus der konkurrierenden Bindungsspaltungen und der Umlagerungsprozesse wird formuliert. Die Wechselwirkung der funktionellen Gruppen sowie deren Einflus auf das Fragmentationsverhalten der Substanzen wird beschrieben und ein Schema der Hauptfragmentierungswege vorgeschlagen. Mess Spectrometry of Reactants for the Synthesis of H2-Active Compounds 4-[(2-Aminoethoxy)methyl]-5-methylimidazole (l), the imidazoles 2-5 with N-substituted ethylene…

H2-Antihistaminika, 7. Mitt. Synthese und H2-antihistaminische Wirkung N,N′-substituierter Thioharnstoffe, Cyanoguanidine und Dithiooxamide

1981

Es wurden N′-substituierte Thioharnstoffe, Cyanoguanidine und Dithiooxamide mit einem 5-Methyl-4-imidazolyl-methylthioethyl-Substituenten dargestellt und auf H2-antihistaminische Wirksamkeit untersucht. H2-Antihistaminics, VII: Synthesis and H2-Antihistaminic Activity of N,N′-Substituted Thioureas, Cyanoguanidines and Dithiooxamides N′-Substituted thioureas, cyanoguanidines and dithiooxamides with a 5-methyl-4-imidazolylmethylthioethyl substituent were prepared and tested for their H2-antihistaminic activity.

ChemInform Abstract: Synthesis and Stereochemical Studies of 2-Substituted Thiazolidine-4-carboxamide Derivatives.

2010

A series of new 2-substituted thiazolidine-4-carboxamide derivatives which have potentially useful immunological properties, have been synthesized in a stereoselective manner by coupling 2-subsituted thiazolidine-4-carboxylic acids with amines or amino esters. The structure of these compounds was established by combination of NMR methods and by X-ray analysis.

CCDC 170383: Experimental Crystal Structure Determination

2002

Related Article: G.Haufe, T.C.Rosen, O.G.J.Meyer, R.Frohlich, K.Rissanen|2002|J.Fluorine Chem.|114|189|doi:10.1016/S0022-1139(02)00040-4

N-(Pyrazin-2-yl)adamantane-1-carboxamide

2016

Molecules of the title compound, C15H19N3O, are composed of an adamantine unit and a pyrazine ring connected to each other through an amide bond. The H—N—C=O moiety is close to planar [C—N—C—O and C—N—C—C torsion angles of 4.7 (2) and −173.8 (1)°, respectively]. The N3—C5 bond has partial double-bond character [1.370 (1) Å]. The geometries of the pyrazine ring and the adamantane substituent are normal and in good agreement with closely related structures. In the crystal, molecules are connected by N—H...O hydrogen bonds, forming zigzag chains in the [001] direction and are arranged in a herringbone fashion.

N,1-Bis(4-ethoxyphenyl)-2,6-dimethyl-4-oxo-1,4-dihydropyridine-3-carboxamide

2018

Condensation of ethyl acetoacetate and phenetidine gives the title compound, C24H26N2O4. The planar ethoxyphenyl group attached to the pyridine ring is twisted about 77.96 (11)° out of the plane of the N-ethoxycarboxamidopyridine unit. The carboxamide unit forms a dihedral angle of about 28.1 (2)° with the pyridine ring.

Crystal structure of 5-{3-[2,6-dimethyl- 4-(5-methyl-1,2,4-oxadiazol-3-yl)phenoxy]propyl}- N-(11-hydroxyundecyl)isoxazole-3-carboxamide hemihydrate

2015

The crystal structure and supra­molecular features of 5-{3-[2,6-dimethyl-4-(5-methyl-1,2,4-oxa­diazol-3-yl)phen­oxy]prop­yl}-N-(11-hy­droxy­undec­yl)isoxazole-3-carboxamide hemihydrate, a derivative of anti­viral ‘WIN compounds’, are reported.

Theoretical prediction of the photoinduced chemiluminescence of pesticides

2007

Although it is relatively easy to find chemiluminescent (CL) molecules working on the field of direct liquid phase (especially employing strong oxidants), the molecules found as chemiluminescent are normally very weak CL compounds for developing suitable analytical CL-procedures. Therefore, it is mandatory to develop new strategies to enhance in a simple way the native chemiluminescence of such a compounds, and even to increase the number of compounds to be determined by direct chemiluminescence. Photoinduced chemiluminescence (Ph-CL) results in a simple and easily on-line accessible strategy to solve these disadvantages. In the present paper, molecular connectivity, a topological method wh…

Reaction of 4-acylaminomethylpyridine N-oxides with phenylbutazone in the presence of acetic anhydride

1987