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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.

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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—H...O hydrogen bonds.

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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—H...O hydrogen bonds along the a axis.

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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—H...O hydrogen bonds.

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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—H...O hydrogen bonds.

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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—H...N hydrogen bonds.

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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—H...O and C—H...O hydrogen bonds.

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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)°.

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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—H...O 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—H...O hydrogen bonds.
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