Methyl 4-anilino-2′,5-dioxo-1′,2′-dihydro-5H-spiro[furan-2,3′-indole]-3-carboxylate
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منابع مشابه
Methyl 4-anilino-2′,5-dioxo-1′,2′-dihydro-5H-spiro[furan-2,3′-indole]-3-carboxylate
In the title compound, C19H14N2O5, the spiro junction links an oxindole moeity and a furan ring, which subtend a dihedral angle of 83.49 (6)°. The mol-ecular structure features an N-H⋯O hydrogen bond, which generates an S(6) ring motif. The crystal packing is governed by two N-H⋯O inter-actions, one of which generates a centrosymmetric R 2 (2)(14) dimer. The other N-H⋯O inter-action along with ...
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In the mol-ecule of the title compound, C(14)H(12)N(2)O(4), the aromatic rings are oriented at a dihedral angle of 51.50 (4)°. An intra-molecular N-H⋯O inter-action results in the formation of a six-membered ring having an envelope conformation. In the crystal structure, inter-molecular N-H⋯O inter-actions link the mol-ecules into centrosymmetric dimers. π-π contacts between the benzene rings [...
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In the title compound, C19H13BrN2O5, the spiro furan ring is almost planar with a maximum deviation of 0.034 (2) Å. The indole unit and the furan ring are normal to each other, making a dihedral angle of 87.82 (8) °. The mol-ecular structure is stabilized by an intra-molecular N-H⋯O hydrogen bond, which generates an S(6) ring motif. In the crystal, mol-ecules are linked via pairs of N-H⋯O hydro...
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There are two independent mol-ecules in the asymmetric unit of the title compound, C(13)H(13)NO(7)S, which have almost identical geometries. The thia-zine ring adopts a sofa conformation in both mol-ecules and the mol-ecular conformations are stabilized by intramolecular O-H⋯O hydrogen bonds. Inter-molecular C-H⋯O hydrogen bonds stabilize the crystal packing.
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In the title compound, C(15)H(14)O(5), an intramolecular O-H⋯O hydrogen bond occurs. In the crystal, the molecules form inversion dimers linked by pairs of O-H⋯O bonds, which are further linked by C-H⋯O interactions.
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ژورنال
عنوان ژورنال: Acta Crystallographica Section E Structure Reports Online
سال: 2013
ISSN: 1600-5368
DOI: 10.1107/s1600536813014967