Gliquidone

Thomas Gelbrich; Mairi F. Haddow; Ulrich J. Griesser

doi:10.1107/S1600536811016680

Gliquidone

Thomas Gelbrich, Mairi F. Haddow, Ulrich J. Griesser

Research output: Contribution to journal › Article (Academic Journal) › peer-review

4 Citations (Scopus)

Abstract

The title compound {systematic name: N-cyclohexylcarbamoyl-4-[2-(7-methoxy-4,4-dimethyl-1,3-dioxo-1,2,3,4-tetrahydroisoquinolin-2-yl)ethyl]benzenesulfonamide}, C27H33N3O6S, displays an intramolecular N-H...O=S interaction, as well as intermolecular N-H...O=C hydrogen bonds. The latter interactions lead to the formation of hydrogen-bonded chains parallel to the c axis. The conformation of the sulfonylurea fragment is in agreement with a recent theoretical study [Kasetti et al. (2010). J. Phys. Chem. B, 114, 11603-11610].

Original language	English
Pages (from-to)	O1343-U2176
Number of pages	11
Journal	Acta Crystallographica Section E: Structure Reports Online
Volume	67
DOIs	https://doi.org/10.1107/S1600536811016680
Publication status	Published - Jun 2011

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@article{712d3634ce934997943cff86bee24ed5,

title = "Gliquidone",

abstract = "The title compound {systematic name: N-cyclohexylcarbamoyl-4-[2-(7-methoxy-4,4-dimethyl-1,3-dioxo-1,2,3,4-tetrahydroisoquinolin-2-yl)ethyl]benzenesulfonamide}, C27H33N3O6S, displays an intramolecular N-H...O=S interaction, as well as intermolecular N-H...O=C hydrogen bonds. The latter interactions lead to the formation of hydrogen-bonded chains parallel to the c axis. The conformation of the sulfonylurea fragment is in agreement with a recent theoretical study [Kasetti et al. (2010). J. Phys. Chem. B, 114, 11603-11610].",

author = "Thomas Gelbrich and Haddow, {Mairi F.} and Griesser, {Ulrich J.}",

year = "2011",

month = jun,

doi = "10.1107/S1600536811016680",

language = "English",

volume = "67",

pages = "O1343--U2176",

journal = "Acta Crystallographica Section E: Structure Reports Online",

issn = "1600-5368",

publisher = "Munksgaard International Publishers",

}

TY - JOUR

T1 - Gliquidone

AU - Gelbrich, Thomas

AU - Haddow, Mairi F.

AU - Griesser, Ulrich J.

PY - 2011/6

Y1 - 2011/6

N2 - The title compound {systematic name: N-cyclohexylcarbamoyl-4-[2-(7-methoxy-4,4-dimethyl-1,3-dioxo-1,2,3,4-tetrahydroisoquinolin-2-yl)ethyl]benzenesulfonamide}, C27H33N3O6S, displays an intramolecular N-H...O=S interaction, as well as intermolecular N-H...O=C hydrogen bonds. The latter interactions lead to the formation of hydrogen-bonded chains parallel to the c axis. The conformation of the sulfonylurea fragment is in agreement with a recent theoretical study [Kasetti et al. (2010). J. Phys. Chem. B, 114, 11603-11610].

AB - The title compound {systematic name: N-cyclohexylcarbamoyl-4-[2-(7-methoxy-4,4-dimethyl-1,3-dioxo-1,2,3,4-tetrahydroisoquinolin-2-yl)ethyl]benzenesulfonamide}, C27H33N3O6S, displays an intramolecular N-H...O=S interaction, as well as intermolecular N-H...O=C hydrogen bonds. The latter interactions lead to the formation of hydrogen-bonded chains parallel to the c axis. The conformation of the sulfonylurea fragment is in agreement with a recent theoretical study [Kasetti et al. (2010). J. Phys. Chem. B, 114, 11603-11610].

U2 - 10.1107/S1600536811016680

DO - 10.1107/S1600536811016680

M3 - Article (Academic Journal)

C2 - 21754738

VL - 67

SP - O1343-U2176

JO - Acta Crystallographica Section E: Structure Reports Online

JF - Acta Crystallographica Section E: Structure Reports Online

SN - 1600-5368

ER -

Gliquidone

Abstract

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