TY - JOUR
T1 - N-benzo[c][1,2,5]thiazol-4-yl-3-trifluoromethylbenzamide
AU - Al Mamari, Hamad H.
AU - Al Awaimri, Nasser
AU - Al Lawati, Yousuf
N1 - Publisher Copyright:
© 2019 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2019/9
Y1 - 2019/9
N2 - The title compound, N-benzo[c][1,2,5]thiazol-4-yl-3-trifluoromethylbenzamide (1) was synthesized by reacting 3-trifluoromethylbenzoyl chloride (4) and 4-aminobenzo[c][1,2,5]thiadiazole (5). The compound was characterized by various spectroscopic methods (1H NMR, 13C NMR, IR, GC-MS) and its composition confirmed by elemental analysis. The importance of this compound lies in its possession of an N,N-bidentate directing group. Such a structural motif is potentially suitable for metal-catalyzed C-H bond functionalization reactions.
AB - The title compound, N-benzo[c][1,2,5]thiazol-4-yl-3-trifluoromethylbenzamide (1) was synthesized by reacting 3-trifluoromethylbenzoyl chloride (4) and 4-aminobenzo[c][1,2,5]thiadiazole (5). The compound was characterized by various spectroscopic methods (1H NMR, 13C NMR, IR, GC-MS) and its composition confirmed by elemental analysis. The importance of this compound lies in its possession of an N,N-bidentate directing group. Such a structural motif is potentially suitable for metal-catalyzed C-H bond functionalization reactions.
KW - Benzamide
KW - Bidentate directing group
KW - C-H functionalization
UR - http://www.scopus.com/inward/record.url?scp=85070375771&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85070375771&partnerID=8YFLogxK
U2 - 10.3390/M1075
DO - 10.3390/M1075
M3 - Comment/debate
AN - SCOPUS:85070375771
SN - 1422-8599
VL - 2019
JO - MolBank
JF - MolBank
IS - 3
M1 - M1075
ER -