Synthesis, characterization, and in vitro microbial evaluation of some new 4H-chromene and quinoline derivatives of 1H-pyrazole

Journal of Heterocyclic Chemistry

Volumn 49, Issue 5, 2012, Pages 1169-1178

  Thumar, Nilesh J ^a   Patel, Manish P ^a  

^a SARDAR PATEL UNIVERSITY   (India)

Author keywords

[No Author keywords available]

Indexed keywords

1H PYRAZOLE; 1H PYRAZOLE 4 CARBALDEHYDE; 2 AMINO 4 (5 CHLORO 3 METHYL 1 PHENYL 1H PYRAZOL 4 YL) 1 [4 (4 FLUOROPHENYL)THIAZOL 2 YL] 5 OXO 1,4,5,6,7,8 HEXAHYDROQUINOLINE 3 CARBONITRILE; 2 AMINO 4 (5 CHLORO 3 METHYL 1 PHENYL 1H PYRAZOL 4 YL) 1 [4 (4 FLUOROPHENYL)THIAZOL 2 YL] 7,7 DIMETHYL 5 OXO 1,4,5,6,7,8 HEXAHYDROQUINOLINE 3 CARBONITRILE; 2 AMINO 4 (5 CHLORO 3 METHYL 1 PHENYL 1H PYRAZOL 4 YL) 5 OXO 1 (4 PHENYLTHIAZOL 2 YL) 1,4,5,6,7,8 HEXAHYDROQUINOLINE 3 CARBONITRILE; 2 AMINO 4 (5 CHLORO 3 METHYL 1 PHENYL 1H PYRAZOL 4 YL) 5 OXO 4,5 DIHYDROPYRANO[3,2 C]CHROMENE 3 CARBONITRILE; 2 AMINO 4 (5 CHLORO 3 METHYL 1 PHENYL 1H PYRAZOL 4 YL) 7,7 DIMETHYL 5 OXO 1 (4 PHENYLTHIAZOL 2 YL) 1,4,5,6,7,8 HEXAHYDROQUINOLINE 3 CARBONITRILE; 2 AMINO 4 (5 CHLORO 3 METHYL 1 PHENYL 1H PYRAZOL 4 YL) 9 METHYL 5 OXO 4,5 DIHYDROPYRANO[3,2 C]CHROMENE 3 CARBONITRILE; 2 AMINO 4 (5 CHLORO 3 METHYL 1,4 TOLYL 1H PYRAZOL 4 YL) 1 [4 (4 FLUOROPHENYL)THIAZOL 2 YL) 5 OXO 1,4,5,6,7,8 HEXAHYDROQUINOLINE 3 CARBONITRILE; 2 AMINO 4 (5 CHLORO 3 METHYL 1,4 TOLYL 1H PYRAZOL 4 YL) 5 OXO 1 (4 PHENYLTHIAZOL 2 YL) 1,4,5,6,7,8 HEXAHYDROQUINOLINE 3 CARBONITRILE; 2 AMINO 4 (5 CHLORO 3 METHYL 1,4 TOLYL 1H PYRAZOL 4 YL) 7,7 DIMETHYL 5 OXO 1 (4 PHENYLTHIAZOL 2 YL) 1,4,5,6,7,8 HEXAHYDROQUINOLINE 3 CARBONITRILE; 2 AMINO 4 (5 CHLORO 3 METHYL 1,4 TOLYL 1H PYRAZOL 4 YL) 9 METHYL 5 OXO 4,5 DIHYDROPYRANO[3,2 C]CHROMENE 3 CARBONITRILE; 2 AMINO 4 [5 CHLORO 1 (3 CHLOROPHENYL) 3 METHYL 1H PYRAZOL 4 YL) 5 OXO 1 (4 PHENYLTHIAZOL 2 YL) 1,4,5,6,7,8 HEXAHYDROQUINOLINE 3 CARBONITRILE; 2 AMINO 4 [5 CHLORO 1 (3 CHLOROPHENYL) 3 METHYL 1H PYRAZOL 4 YL] 1 [4 (4 FLUOROPHENYL)THIAZOL 2 YL] 5 OXO 1,4,5,6,7,8 HEXAHYDROQUINOLINE 3 CARBONITRILE; 2 AMINO 4 [5 CHLORO 1 (3 CHLOROPHENYL) 3 METHYL 1H PYRAZOL 4 YL] 5 OXO 4,5 DIHYDROPYRANO[3,2 C]CHROMENE 3 CARBONITRILE; 2 AMINO 4 [5 CHLORO 1 (3 CHLOROPHENYL) 3 METHYL 1H PYRAZOL 4 YL] 9 METHYL 5 OXO 4,5 DIHYDROPYRANO[3,2 C]CHROMENE 3 CARBONITRILE; 2 AMINO 9 CHLORO 4 (5 CHLORO 3 METHYL 1 PHENYL 1H PYRAZOL 4 YL) 5 OXO 4,5 DIHYDROPYRANO[3,2 C]CHROMENE 3 CARBONITRILE; 2 AMINO 9 CHLORO 4 (5 CHLORO 3 METHYL 1,4 TOLYL 1H PYRAZOL 4 YL) 5 OXO 4,5 DIHYDROPYRANO[3,2 C]CHROMENE 3 CARBONITRILE; 2 AMINO 9 CHLORO 4 [5 CHLORO 1 (3 CHLOROPHENYL) 3 METHYL 1H PYRAZOL 4 YL] 5 OXO 4,5 DIHYDROPYRANO[3,2 C]CHROMENE 3 CARBONITRILE; 4 HYDROXY COUMARIN; ANTIINFECTIVE AGENT; BETA ENAMINONE DERIVATIVE; CHROMENE DERIVATIVE; MALONONITRILE; PYRAZOLE DERIVATIVE; QUINOLINE DERIVATIVE; UNCLASSIFIED DRUG;

ANTIMICROBIAL ACTIVITY; ARTICLE; BACILLUS SUBTILIS; CARBON NUCLEAR MAGNETIC RESONANCE; CATALYSIS; CLOSTRIDIUM TETANI; CONTROLLED STUDY; CYCLOCONDENSATION REACTION; DRUG STRUCTURE; DRUG SYNTHESIS; IN VITRO STUDY; INFRARED SPECTROSCOPY; NONHUMAN; POLYMERIZATION; PROTON NUCLEAR MAGNETIC RESONANCE;

EID: 84868099752     PISSN: 0022152X     EISSN: 19435193     Source Type: Journal    
DOI: 10.1002/jhet.1038     Document Type: Article

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