TY - JOUR
T1 - Crystal structures of three substituted 3-aryl-2-phenyl-2,3-dihydro-4H-1,3-benzothiazin-4-ones
AU - Yennawar, Hemant P.
AU - Coyle, David J.
AU - Noble, Duncan J.
AU - Yang, Ziwei
AU - Silverberg, Lee J.
PY - 2016/8/1
Y1 - 2016/8/1
N2 - Three ring-substituted 3-aryl analogs of 2-phenyl-2,3-dihydro-4H-1,3-benzothiazin-4-one, namely 3-(4-methoxyphenyl)-2-phenyl-4H-1,3-benzothiazin-4-one, C21H17NO2S, (I), 2-phenyl-3-[4-(trifluoromethyl)phenyl]-2,3-dihydro-4H-1,3-benzothiazin-4-one toluene hemisolvate, C21H14F3NOS·0.5C7H8, (II), and 3-(3-bromophenyl)-2-phenyl-2,3-dihydro-4H-1,3-benzothiazin-4-one toluene hemisolvate, C20H14BrNOS·0.5C7H8, (III), were synthesized and their crystal structures determined. The hemisolvates differ in that in (II), the asymmetric unit comprises two molecules of the benzothiazinone compound and a toluene solvent molecule, whereas in (III), the unit comprises one benzothiazinone molecule and a half-occupancy toluene solvent molecule. All crystals are of racemic mixtures of the chiral 2-C atom of the thiazine moiety, which in all structures has a screw-boat puckering, with the puckering amplitude values within the range 0.575-0.603Å. In all three structures, the benzene plane of the benzothiazine system makes a dihedral angle in the range 78.60(5) to 98.40(5)° with the unsubstituted benzene plane and in the range 70.50(1) to 121.00(5)° with the substituted benzene plane. The CF3 substituent group in one of the molecules of (II) shows positional disorder, with an occupancy ratio of 0.57(3):0.43(3). In the crystals of (I) and (II), weak intermolecular C - H···O interactions are present, giving in (I), molecules arranged in a plane parallel to (010), and in (II), chains along a. In addition, all three structures show weak C - H···π interactions involving various aromatic rings.
AB - Three ring-substituted 3-aryl analogs of 2-phenyl-2,3-dihydro-4H-1,3-benzothiazin-4-one, namely 3-(4-methoxyphenyl)-2-phenyl-4H-1,3-benzothiazin-4-one, C21H17NO2S, (I), 2-phenyl-3-[4-(trifluoromethyl)phenyl]-2,3-dihydro-4H-1,3-benzothiazin-4-one toluene hemisolvate, C21H14F3NOS·0.5C7H8, (II), and 3-(3-bromophenyl)-2-phenyl-2,3-dihydro-4H-1,3-benzothiazin-4-one toluene hemisolvate, C20H14BrNOS·0.5C7H8, (III), were synthesized and their crystal structures determined. The hemisolvates differ in that in (II), the asymmetric unit comprises two molecules of the benzothiazinone compound and a toluene solvent molecule, whereas in (III), the unit comprises one benzothiazinone molecule and a half-occupancy toluene solvent molecule. All crystals are of racemic mixtures of the chiral 2-C atom of the thiazine moiety, which in all structures has a screw-boat puckering, with the puckering amplitude values within the range 0.575-0.603Å. In all three structures, the benzene plane of the benzothiazine system makes a dihedral angle in the range 78.60(5) to 98.40(5)° with the unsubstituted benzene plane and in the range 70.50(1) to 121.00(5)° with the substituted benzene plane. The CF3 substituent group in one of the molecules of (II) shows positional disorder, with an occupancy ratio of 0.57(3):0.43(3). In the crystals of (I) and (II), weak intermolecular C - H···O interactions are present, giving in (I), molecules arranged in a plane parallel to (010), and in (II), chains along a. In addition, all three structures show weak C - H···π interactions involving various aromatic rings.
UR - http://www.scopus.com/inward/record.url?scp=84982943773&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84982943773&partnerID=8YFLogxK
U2 - 10.1107/S2056989016011002
DO - 10.1107/S2056989016011002
M3 - Article
AN - SCOPUS:84982943773
SN - 2056-9890
VL - 72
SP - 1108
EP - 1112
JO - Acta Crystallographica Section E: Crystallographic Communications
JF - Acta Crystallographica Section E: Crystallographic Communications
ER -