83548-57-6

Upstream product

• 18002-03-4 2-benzyl-5,6-tetramethylenethieno<2,3-d>pyrimidin-4(3H)-one 
• 103-81-1 Benzeneacetamide 
• 645-54-5 2-phenylthioacetamide 
• 140-29-4 phenylacetonitrile 
• 4506-71-2 ethyl 2-amino-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate 
• 18002-03-4 2-benzyl-5,6,7,8-tetrahydro-3H-benzo[4,5]thieno[2,3-d]pyrimidin-4-one 

Downstream Products

• 401511-15-7 2-benzyl-4-[(2-hydroxy)ethyl]amino-5,6,7,8-tetrahydrobenzo(b)thieno[2,3-d]pyrimidine 
• 947328-95-2 2-benzyl-4-[(3-hydroxy)propyl]amino-5,6,7,8-tetrahydrobenzo[b]thieno[2,3-d]pyrimidine 
• 83548-64-5 (2-Benzyl-5,6,7,8-tetrahydro-benzo[4,5]thieno[2,3-d]pyrimidin-4-yl)-hydrazine 
• 423128-56-7 2-benzyl-4-(4-methylpiperazin-1-yl)-5,6,7,8-tetrahydrobenzo[4,5]-thieno[2,3-d]pyrimidine 
• 83548-71-4 4-Benzyl-7,8,9,10-tetrahydro-6-thia-1,2,3,3a,5-pentaaza-cyclopenta[c]fluorene 

Relevant academic research and scientific papers

Microwave-assisted synthesis of potent PDE7 inhibitors containing a thienopyrimidin-4-amine scaffold

A series of novel thienopyrimidin-4-amines have been synthesized and evaluated as phosphodiesterase (PDE) inhibitors. A rationale for the observed selectivity against PDE7 has been obtained from molecular modelling studies on the most active compounds. This journal is the Partner Organisations 2014.

Multistep, microwave assisted, solvent free synthesis and antibacterial activity of 6-substituted-2,3,4-trihydropyrimido[1,2-c]9,10,11,12- tetrahydrobenzo[b]thieno[3,2-e]pyrimidines

A novel, efficient, microwave assisted route for the synthesis of 6-substituted-2,3,4-trihydropyrimido[1,2-c]-9,10,11,12-tetrahydrobenzo[b] thieno[3,2-e]pyrimidines in good yields has been developed. The intermediates, 2-substituted-4-[3-hydroxy(propyl-1-

Microwave-Assisted Synthesis of Novel 5-Substituted-2,3-dihydroimidazo[1,2-c]thieno[3,2-e]pyrimidines

A novel, facile microwave-assisted route for the synthesis of imidazo[1,2-c]thieno[3,2-e]pyrimidines 4 in quantitative yields is reported. The intermediates 4-chlorothieno[2,3-d]pyrimidines 3 were synthesized under one-pot reaction conditions.

Synthesis and Biological Activity of Tetrazolothienopyrimidines

4-Hydrazinothienopyrimidines (VI) undergo cyclization with nitrous acid to give tetrazolothienopyrimidines (VII).The latter compounds have been screened for their analgesic and antiinflammatory activities.