1027003-73-1

Upstream product

• 1004-40-6 6-Amino-2-thiouracil 
• 42792-80-3 2,6-bis(4-chlorobenzylidene)cyclohexanone 
• 108-94-1 cyclohexanone 
• 104-88-1 4-chlorobenzaldehyde 

Downstream Products

• 1027003-76-4 5-(4-chlorophenyl)-9-(4-chlorophenylmethylene)-2-hydrazino-6,7,8,9-tetrahydropyrimido[4,5-b]quinolin-4(3H)-one 
• 1180512-06-4 3-amino-6-(4-chlorophenyl)-10-(4-chlorophenylmethylene)-5-oxo-7,8,9,10-tetrahydrothiazolo[3',2':1,2]pyrimido[4,5-b]quinoline-2-carbonitrile 
• 1027003-75-3 5-(4-chlorophenyl)-9-(4-chlorophenylmethylene)-2-methylthio-6,7,8,9-tetrahydropyrimido[4,5-b]-quinolin-4-one 
• 1145713-23-0 2-(S-phenacyl)-5-(4-chlorophenyl)-9-(4-chlorophenylmethylene)-6,7,8,9-tetrahydropyrimido[4,5-b]quinolin-4-one 
• 1145713-21-8 2-(acetylacetonethio)-5-(4-chlorophenyl)-9-(4-chlorophenylmethylene)-6,7,8,9-tetrahydropyrimido[4,5-b]quinolin-4-one 
• 1145713-13-8 6-(4-chlorophenyl)-10-(4-chlorophenylmethylene)-2-(4-N,N-dimethyl-aminophenylmethylene)-7,8,9,10-tetrahydrothiazolo-[3',2':1,2]pyrimido[4,5-b]quinoline-3,5-dione 
• 1145713-15-0 6-(chlorophenyl)-10-(4-chlorophenylmethylene)-7,8,9,10-tetrahydrothiazolo[3',2':1,2]pyrimido[4,5-b]quinoline-3,5-dione 
• 1145713-22-9 2-(S-acetone)-5-(4-chlorophenyl)-9-(4-chlorophenylmethylene)-6,7,8,9-tetrahydropyrimido[4,5-b]quinolin-4-one 
• 1145713-20-7 5-(4-chlorophenyl)-9-(4-chlorophenylmethylene)-2-ethylthio-6,7,8,9-tetrahydropyrimido[4,5-b]-quinolin-4-one 
• 1145713-11-6 6-(4-chlorophenyl)-10-(4-chlorophenylmethylene)-2-(4-methoxyphenylmethylene)-7,8,9,10-tetrahydrothiazolo-[3',2':1,2]pyrimido[4,5-b]quinoline-3,5-dione 
• 1145713-07-0 6-(4-chlorophenyl)-10-(4-chlorophenylmethylene)-2-phenylmethylene-7,8,9,10-tetrahydrothiazolo-[3',2':1,2]pyrimido[4,5-b]quinoline-3,5-dione 
• 1145713-12-7 6-(4-chlorophenyl)-10-(4-chlorophenylmethylene)-2-(2-thienyl-methylene)-7,8,9,10-tetrahydrothiazolo-[3',2':1,2]pyrimido[4,5-b]quinoline-3,5-dione 

Relevant academic research and scientific papers

Synthesis and antioxidant, anti-inflammatory, and analgesic activity of novel polycyclic pyrimido[4,5-b]quinolines

The behavior of the 2-methylthio-pyrimido[4,5-b]quinolin-4-one towards differently substituted amines is reported. Also, the reactivity of 3-aminothiazolo[3′,2′ :1,2]-pyrimido[4,5-b]quinoline-2-carbonitrile towards formic acid, urea, thiourea, formamide,

New acyclic nucleosides analogues as potential analgesic, anti-inflammatory, anti-oxidant and anti-microbial derived from pyrimido[4,5-b]quinolines

Synthesis of 2-thioxopyrimido[4,5-b]quinoline 3a-c by microwave oven was used as a base to synthesis acyclic nucleosides analogue of types, 3-(penta-O-acetyl-glycosyl)-6-(4-chlorophenyl)-10-(4-chlorophenylmethyle ne)-7,8,9,10-tetrahydro[1,2,4]triazolo[4′,

Design and synthesis of azolopyrimidoquinolines, pyrimidoquinazolines as anti-oxidant, anti-inflammatory and analgesic activities

The 5,10-dihydro-2-thioxo-pyrimido[4,5-b]quinolines (2a-c) and its oxidized form 3 were prepared and used as key intermediates for the synthesis of thiazolo[3′,2′:1,2]pyrimido[4,5-b]-quinolines (5a-c), isoxazolo[5″,4″:4′,5′]thiazolo[3′,2′:1,2]pyrimido[4,5