A convenient synthesis of 2-arylidene-5H-thiazolo[2,3-b]quinazoline-3,5[2H]-diones and their benzoquinazoline derivatives

Journal of Heterocyclic Chemistry

Volumn 39, Issue 6, 2002, Pages 1153-1160

  Khodair, Ahmed I ^a,b  

^a TANTA UNIVERSITY   (Egypt)

^b UNIVERSITY OF KONSTANZ   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

2 (2 ACETOXY 3 METHOXYBENZYLIDENE) 5H THIAZOLO[2,3 B]BENZOQUINAZOLINE 3,5(2H) DIONE; 2 (2 ACETOXY 3 METHOXYBENZYLIDENE) 5H THIAZO[2,3 B]QUINAZOLINE 3,5(2H) DIONE; 2 (2 ACETOXY 3 METHOXYBENZYLIDENE) 7,8 DIMETHOXY 5H THIAZOLO[2,3B]QUINAZOLINE 3,5(2H) DIONE; 2 (2 FURYLIDENE) 5H THIAZOLO[2,3 B]QUINAZOLINE 3,5(2H) DIONE; 2 (2 THIENYLIDENE) 5H THIAZOLO[2,3 B]QUINAZOLINE 3,5(2H) DIONE; 2 (4 ACETOXYBENZYLIDENE) 5H THIAZOLO[2,3 B]QUINAZOLINE 3,5(2H) DIONE; 2 (4 METHOXYBENZYLIDENE) 5H THIAZOLO[2,3B]QUINAZOLINE 3,5(2H) DIONE; 2 (4 METHOXYBENZYLIDENE) 7 CHLORO 5H THIAZOLO[2,3 B]QUINAZOLINE 3,5(2H) DIONE; 2 (4 METHOXYBENZYLIDENE) 7,8 DIMETHOXY 5H THIAZOLO[2,3B]QUINAZOLINE 3,5 (2H) DIONE; 2 (BENZYLIDENE) 5H THIAZOLO[2,3 B]BENZOQUINAZOLINE 3,5(2H) DIONE; 2 (BENZYLIDENE) 5H THIAZOLO[2,3 B]QUINAZOLINE 3,5(2H) DIONE; 2 (BENZYLIDENE) 7 BROMO 5H THIAZOLO[2,3 B]QUINAZOLINE 3,5(2H) DIONE; 2 (BENZYLIDENE) 7 CHLORO 5H THIAZOLO[2,3 B]QUINAZOLINE 3,5(2H) DIONE; 5H THIAZOLO[2,3 B]QUINAZOLINE 3,5(2H) DIONE; 6 CHLORO 2 (2 THIENYLIDENE) 5H THIAZOLO[2,3 B]QUINAZOLIEN 3,5(2H) DIONE; 7 BROMO 2 (2 FURYLIDENE) 5H THIAZOLO[2,3 B]QUINAZOLINE 3,5(2H) DIONE; 7 CHLORO 2 (2 FURYLIDENE) 5H THIAZOLO[2,3 B]QUINAZOLINE 3,5(2H) DIONE; 7,8 DIMETHOXY 2 (2 THIENYLIDENE) 5H THIAZOLO[2,3 B]QUINAZOLINE 3,5(2H) DIONE; 7,8 DIMETHOXY 5H THIAZOLO[2,3 B]QUINAZOLINE 3,5(2H) DIONE; BENZOQUINAZOLINE DERIVATIVE; QUINAZOLINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL REACTION; DRUG STRUCTURE; DRUG SYNTHESIS; INFRARED SPECTROSCOPY; POLYMERIZATION; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; STRUCTURE ANALYSIS;

EID: 0036875592     PISSN: 0022152X     EISSN: None     Source Type: Journal    
DOI: 10.1002/jhet.5570390607     Document Type: Article

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