2019
DOI: 10.1107/s2056989019003864
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Crystal structure of diethyl 2-amino-5-{4-[bis(4-methylphenyl)amino]benzamido}thiophene-3,4-dicarboxylate

Abstract: In the title compound, C31H31N3O5S, the regioselective substitution of the thiophene is confirmed with the amine and the amide at the 2- and 5-positions, respectively. In the molecule, the thiophene ring is twisted by 12.82 (3)° with respect to the aromatic ring of the benzamido group. Intramolecular N—H...O hydrogen bonds are present involving the N atoms of the primary amine and the amide groups, forming S(6) ring motifs. In the crystal, centrosymmetrically related molecules are linked by pairs of N—H...O hy… Show more

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Cited by 4 publications
(5 citation statements)
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“…2A formed two intramolecular bondsone between each of the terminal amines with the adjacent ester carbonyl N1···O2 and N4···O7 (Figure A). This is consistent with similar structures, and it results in an S6-type supramolecular cycle. The crystallographic structure also confirmed that 2A formed intermolecular contacts.…”
Section: Resultssupporting
confidence: 90%
See 1 more Smart Citation
“…2A formed two intramolecular bondsone between each of the terminal amines with the adjacent ester carbonyl N1···O2 and N4···O7 (Figure A). This is consistent with similar structures, and it results in an S6-type supramolecular cycle. The crystallographic structure also confirmed that 2A formed intermolecular contacts.…”
Section: Resultssupporting
confidence: 90%
“…33 In fact, it is 0.03 Å longer than the corresponding NC bond and 0.06 Å shorter than the 2A). This is consistent with similar structures, 34 and it results in an S6-type supramolecular cycle. The crystallographic structure also confirmed that 2A formed intermolecular contacts.…”
Section: Resultsmentioning
confidence: 99%
“…19 In fact, the nitrogens of the amine and amide of 3 formed both intra- and intermolecular bonds, resulting in a head-to-head supramolecular dimer. 20 1D also formed hydrogen bonds (Fig. 2B and Table 1).…”
Section: Resultsmentioning
confidence: 94%
“…[51] Since its introduction, the MetalJet X-ray source has been used in single crystal X-ray diffraction studies involving all kinds of different compounds. From small organic molecules [59][60][61][62][63][64] to proteins, [65][66][67][68] polymers [69,70] and metal organic frameworks. [71] Furthermore inorganic compounds containing p-block elements [72,73] as well as d-metal complexes [74][75][76][77][78][79][80] have been investigated.…”
Section: Metaljet X-ray Sourcementioning
confidence: 99%
“…A set of objects prepared in this way and a laboratory stand at hand, in principle all types of screw axes can be modelled, if the correct number of ducks is arranged in a suitable manner. With certain screw axes (42,62,63,64) two or more objects occupy positions at the same height. To be able to accurately model this, special mounts were designed, which have several pieces of sheet metal attached to the same aluminium block (see Figure 2 -18).…”
Section: Screw Axesmentioning
confidence: 99%