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Synthesis and antiviral activity of novel pyrazole amides containing α‐aminophosphonate moiety
Author(s) -
Wu Lintao,
Song Baoan,
Bhadury Pinaki S.,
Yang Song,
Hu Deyu,
Jin Linhong
Publication year - 2011
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.591
Subject(s) - moiety , chemistry , enantiomer , pyrazole , bioassay , combinatorial chemistry , stereochemistry , biology , genetics
Abstract A series of novel pyrazole amides J1 , J2 , J3 , J4 , J5 , J6 , J7 , J8 , J9 , J10 , J11 , J12 , J13 , J14 , J15 containing an α‐aminophosphonate moiety were synthesized and subsequently characterized by spectral (IR, 1 H‐, 13 C‐, 31 P‐, and 19 F‐NMR) data and elemental analysis. The racemic sample of J1 was further separated into its enantiomers under normal‐phase condition on two immobilized polysaccharide‐based chiral stationary phases (Chiralpak IA and Chiralpak IC). The synthesized compounds revealed certain degree of antiviral activity in the bioassay. The title compounds ( J3 , J10 , and J12 ) showed some curative activities (39.9%, 41.8%, 50.1%, respectively) against tobacco mosaic virus at 0.5 mg/mL. J. Heterocyclic Chem., 00 , 00 (2011).