organic compounds
The title compound, C15H5Cl4NO3, was synthesized from tetrachlorophthalic anhydride and 4-aminobenzaldehyde. In the molecule, the tetrachlorophthalimide unit is nearly planar and makes a dihedral angle of 56.20 (3)° with the benzene ring.
organic compounds
The title compound, C41H32Cl4N4O2S, was synthesized by the intermolecular [3 + 2] cycloaddition of azomethine ylide, derived from isatin and sarcosine by a decarboxylative route, and 5-(4-chloro)phenyl-10-(4-chloro)benzylidene-2-(2,4-dichloro)benzylidene-2,3,6,7,8,9-hexahydro-5H,10H-cyclohepteno[1,2-d]thiazolo[3,2-a]pyrimidin-3-one. In the molecule, the two spiro junctions link a planar 2-oxindole ring, a pyrrolidine ring in an envelope conformation and a 10-(arylmethylene)hexahydrocyclohepteno[1,2-d]thiazolo[3,2-a]pyrimidin-3-one ring. The packing of the molecules in the crystal structure is mainly due to N—HO hydrogen bonds.
organic compounds
The title compound, C13H10N2O2, is approximately planar in the solid state and displays a trans configuration with respect to the azo double bond. Molecules form infinite chains linked by O—HO hydrogen bonds along the a axis.
organic compounds
The title compound, C48H44N6O2S·2C2H3N, was synthesized by the intermolecular [3+2]-cycloaddition of an azomethine ylide, derived from isatin and sarcosine by a decarboxylative route, and 7-benzyl-9-benzylidene-2-[4-(dimethylamino)benzylidene]-5-phenyl-2,3,6,7,8,9-hexahydro-5H-pyrido[4,3-d]thiazolo[3,2-a]pyrimidin-3-one. In the molecule, the two spiro junctions link a planar 2-oxindole system, a pyrrolidine ring in an envelope conformation and a thiazolidone ring of the fused pyrimidine ring system. The packing of the molecules in the crystal structure is mainly stabilized by N—HO hydrogen bonds.
organic compounds
The structure of the centrosymmetric title compound, C8H6Cl2N2O2·2C3H7NO, shows that the hydroximoyl chloride substituent has an essentially planar arrangement and the dihedral angle between this plane and the benzene plane is 18.3 (4)°. The hydroximoyl chloride group has a cis configuration. The packing can be described as a polymeric arrangement of molecules linked through O—HO hydrogen bonds.
organic compounds
The title compound, C44H42N4O5S, was synthesized by the intermolecular [3+2] cycloaddition of an azomethine ylide, derived from isatin and sarcosine by a decarboxylative route, and 5-(4-methoxyphenyl-10-(4-methoxy)benzylidene-2-(4-methoxy)benzylidene-2,3,6,7,8,9-hexahydro-5H,10H-cyclohepta[1,2-d]thiazolo[3,2-a]pyrimidin-3-one. In the molecule, the two spiro junctions link a planar 2-oxindole ring, a pyrrolidine ring in an envelope conformation and a 10-(arylmethylene)hexahydrocyclohepta[1,2-d]thiazolo[3,2-a]pyrimidin-3-one ring. The packing of the molecules in the crystal structure is mainly governed by N—HN hydrogen bonds.
organic compounds
The title compound, C13H11N3O, is essentially planar in the solid state and displays a trans configuration with respect to the azo double bond. The dihedral angle between the planes of the two aromatic rings is 4.9 (4)°. Molecules form infinite chains via N—HO and C—HO hydrogen bonds.
organic compounds
The title compound, C28H27ClN2O7·0.5C4H10O, was synthesized from ethyl 3-amino-4-[2-(phthalimido)ethoxy]crotonate and methyl 2-(2-chlorobenzylidene)acetoacetate by the Hantzsch reaction. The dihydropyridine ring is not planar, but adopts a boat conformation. The dihedral angle between the phthalimide and 2-chlorophenyl ring planes is 66.0 (3)°.
organic compounds
The crystal structure of the title compound, C17H12N2O2·C10H8O, shows that the molecules are effectively planar in the solid state and the compound exists in the hydrazone form and not the azo form. The hydrazone H atom and carbonyl O atom are linked by an intramolecular N—HO hydrogen bond. The 2-naphthol molecules are disordered over inversion centres, the asymmetric unit containing half each of two such molecules. The packing can be described as a polymeric arrangement of molecules linked through O—HO hydrogen bonds.