434293-29-5

Upstream product

• 105-39-5 chloroacetic acid ethyl ester 
• 83236-50-4 4-<4-chlorophenyl>-3-cyano-5,6-trimethylenepyridine-2<1H>-thione 
• 536720-16-8 [4-(4-chloro-phenyl)-3-cyano-6,7-dihydro-5H-[1]pyrindin-2-ylsulfanyl]-acetic acid ethyl ester 

Downstream Products

• 906375-55-1 3-amino-4-(4-chlorophenyl)-6,7-dihydro-5H-cyclopenta[e]thieno[2,3-b]pyridine-2-carboxylic acid 
• 906375-56-2 4-(4-chloro-phenyl)-6-methyl-2,3-dihydro-1H-7-oxa-9-thia-5,10-diaza-cyclopenta[b]fluoren-8-one 
• 906375-70-0 8-chloro-4-(4-chloro-phenyl)-6-methyl-2,3-dihydro-1H-9-thia-5,7,10-triaza-cyclopenta[b]fluorene 
• 499142-21-1 4-(4-chloro-phenyl)-6-methyl-2,3-dihydro-1H,7H-9-thia-5,7,10-triaza-cyclopenta[b]fluoren-8-one 
• 906375-77-7 [4-(4-chloro-phenyl)-6-methyl-2,3-dihydro-1H-9-thia-5,7,10-triaza-cyclopenta[b]fluoren-8-yl]-hydrazine 

Relevant academic research and scientific papers

Synthesis and reactions of some new heterocyclic compounds containing cycloalka[e]thieno[2,3-b]pyridine Moiety

Hydrolysis of ethyl 3-amino-4-aryl-cycloalka[e]thieno[2,3-b]pyridine-2- carboxylates (3a-d) gave the corresponding o-aminocarboxylic acids 4 a-d. Heating the latter compounds (4a-d) with acetic an hydride furnished the oxazinone derivatives 5a-d which, in