70696-35-4

Upstream product

• 58255-18-8 N-methyl-1-(thiophen-2-yl)methanamine 
• 1122-91-4 4-bromo-benzaldehyde 
• 1003-09-4 2-bromothiophene 
• 1431664-66-2 C₁₀H₁₂BrNO 
• 99-73-0 para-bromophenacyl bromide 

Downstream Products

• 88013-63-2 4-(4-bromophenyl)-6-methyl-2-nitro-4,5,6,7-tetrahydrothieno<2,3-c>pyridine 
• 90553-53-0 4-(4-bromophenyl)-2-tert-butyl-6-methyl-4,5,6,7-tetrahydrothieno<2,3-c>pyridine 
• 88013-55-2 2-(methoxy-methyl)-4-(p-bromo-phenyl)-6-methyl-4,5,6,7-tetrahydro-thieno[2,3-c]pyridine 
• 88013-36-9 2-amino-4-(4-bromophenyl)-6-methyl-4,5,6,7-tetrahydrothieno<2,3-c>pyridine 
• 90553-47-2 4-(4-bromophenyl)-2-(chloromethyl)-6-methyl-4,5,6,7-tetrahydrothieno<2,3-c>pyridine hydrochloride 
• 70696-52-5 4-(4-bromophenyl)-6-methyl-4,5,6,7-tetrahydrothieno<2,3-c>pyridine 

Relevant academic research and scientific papers

Reaction of 5-aryloxazolidines with arylmagnesium bromides as a new route to N-benzyl-β-hydroxyphenethylamines as starting materials for the preparation of 4-aryl-1,2,3,4-tetrahydroisoquinolines

Benzaldehydes react smoothly with the non-stabilized azomethine ylide derived from sarcosine and formaldehyde to form 5-aryloxazolidines as intermediates, which undergo ring-opening to give N-benzyl-β- hydroxyphenethylamines in good yields by the action o

Synthesis and antidepressant activity of 4-aryltetrahydrothieno[2,3-c]pyridine derivatives

A series of substituted 4-aryltetrahydrothieno[2,3-c]pyridines was prepared by acid-catalyzed cyclization of 1-aryl-2-[(2-thienylmethyl)amino]ethanol derivatives. The compounds were examined for their antidepressant activity, as demonstrated by their abil