N-Benzyl-4-methyl-N-(4-methylphenyl)benzenesulfonamide
نویسندگان
چکیده
منابع مشابه
N-Benzyl-4-methyl-N-(4-methylphenyl)benzenesulfonamide
In the title mol-ecule, C(21)H(21)NO(2)S, the phenyl ring makes the dihedral angles of 74.13 (11) and 80.16 (11)° with the two benzene rings, which are inclined at an angle of 43.73 (10)° with respect to each other. In the crystal, mol-ecules are linked by inter-molecular C-H⋯O hydrogen bonds along the [010] direction. In addition, a weak C-H⋯π (arene) inter-action is observed.
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In the crystal structure of the title compound, C(18)H(22)N(2)O(2), the pyridine ring makes dihedral angles of 83.71 (6) and 9.2 (1)° with the phenyl ring and the carbamate plane, respectively. The phenyl ring and the carbamate plane are nearly perpendicular to one another, with a dihedral angle of 87.17 (7)°.
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The mol-ecule of the title compound, C(15)H(17)NO(2)S, has a C-S-N-C torsion angle of 71.4 (2)°, and the dihedral angle between the benzene rings is 82.83 (16)°. In the crystal, mol-ecules are linked into chains along the b axis via C-H⋯O hydrogen bonds. A C-H⋯π inter-action is also present in the crystal structure.
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In the title compound, C(18)H(17)N(3), the dihedral angles between the central pyrimidine ring and its directly-bonded and N-bonded pendant phenyl rings are 25.48 (6) and 80.33 (6)°, respectively. The dihedral angle between the phenyl rings is 79.66 (6)°. In the crystal, inversion dimers linked by pairs of N-H⋯N hydrogen bonds generate R(2) (2)(8) loops. The crystal structure also features weak...
متن کاملN-Benzyl-N-cyclohexyl-4-methylbenzenesulfonamide
In the title compound, C(20)H(25)NO(2)S, the cyclo-hexyl ring exists in a chair form and the mean plane through all six atoms makes dihedral angles of 56.12 (9) and 55.19 (10)° with the benzene and phenyl rings, respectively. The dihedral angle between the two aromatic rings is 77.23 (7)°. A weak intra-molecular C-H⋯O interaction occurs.
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ژورنال
عنوان ژورنال: Acta Crystallographica Section E Structure Reports Online
سال: 2011
ISSN: 1600-5368
DOI: 10.1107/s1600536811028522