Synthesis and crystal structures of <i>N</i>-(2,3,4,6<i>-</i>Tetra-<i>O</i>-acetyl-<i>β</i>-<i>D</i>-glycosyl)thiocarbamoyl <span style="font-size:12.0pt;line-height:115%;font-family:"Times New Roman"; mso-fareast-font-family:"Times New Roman";mso-ansi-language:NL;mso-fareast-language: EN-IN;mso-bidi-language:HI" lang="NL">methylene diamine</span>

Abstract

The structure of <i>N</i>-(2,3,4,6<i>-</i>Tetra-<i>O</i>-acetyl-<i>β</i>-<i>D</i>-glycosyl)thiocarbamoyl methylene diamine, C₁₆H₂₅N₃O₉S has been determined by X-ray diffraction method. It crystallizes in the

monoclinic system, space group P2_l, with lattice parameters a = 7.6560(2), b = 10.3113(3), c = 14.1813(1)Å, β = 100.879 (2)^o, and Z = 2. The hexapyranosyl ring adopts a chair conformation. All the ring substituents are in the equatorial position. The acetoxylmethyl group is in the <i>gauche- gauche</i> conformation. The S atom is in synperiplanar conformation, while the N-C-N-C linkage is antiperiplanar. The N-H^...O intermolecular hydrogen bonds link the molecules into infinite chains and these are connected by C-H^...O interaction.