77302-61-5

Upstream product

• 7720-39-0 1H-imidazol-2-amine 
• 51608-60-7 N-(benzylidene)-p-methylbenzenesulfonamide 
• 100-52-7 benzaldehyde 
• 42383-61-9 2-aminoimidazolesulfate 

Downstream Products

• 1332482-10-6 (5S,6S,7R)-5-(furan-2-yl)-7-phenyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyrimidine-6-carbaldehyde 
• 1332482-11-7 (5S,6S,7R)-7-phenyl-5-(thiophen-2-yl)-5,6,7,8-tetrahydroimidazo[1,2-a]pyrimidine-6-carbaldehyde 
• 1332482-01-5 (5S,6S,7R)-5-(3-chlorophenyl)-7-phenyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyrimidine-6-carbaldehyde 
• 1351353-63-3 ((5S,6S,7R)-5,7-diphenyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyrimidin-6-yl)methanol 
• 1351353-64-4 ((5S,6S,7R)-7-phenyl-5-m-tolyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyrimidin-6-yl)methanol 
• 1351353-89-3 ((5S,6S,7R)-5-(3-methoxyphenyl)-7-phenyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyrimidin-6-yl)methanol 
• 1351353-91-7 ((5S,6S,7R)-5-(3-chlorophenyl)-7-phenyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyrimidin-6-yl)methanol 
• 1351353-94-0 ((5S,6S,7R)-5-(3-bromophenyl)-7-phenyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyrimidin-6-yl)methanol 
• 1351353-95-1 ((5S,6S,7R)-5-(3-nitrophenyl)-7-phenyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyrimidin-6-yl)methanol 
• 1351354-39-6 ((5S,6S,7R)-7-phenyl-5-p-tolyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyrimidin-6-yl)methanol 
• 1351354-47-6 ((5S,6S,7R)-5-(4-methoxyphenyl)-7-phenyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyrimidin-6-yl)methanol 
• 1351354-49-8 ((5S,6S,7R)-5-(4-chlorophenyl)-7-phenyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyrimidin-6-yl)methanol 
• 1351354-72-7 ((5S,6S,7R)-5-(4-bromophenyl)-7-phenyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyrimidin-6-yl)methanol 
• 1351355-35-5 ((5S,6S,7R)-5-(4-nitrophenyl)-7-phenyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyrimidin-6-yl)methanol 

Relevant academic research and scientific papers

Three-component mannich-like reaction of 2-aminoimidazole

A three-component reaction of 2-aminoimidazole with various aldehydes and amines is described that generates 4-substituted 2-aminoimidazoles containing a new chiral centre, a new CC bond and a new CN bond. The reactions can be conducted in water and requi

Organocatalytic asymmetric domino aza-michael - Mannich reaction: Synthesis of tetrahydroimidazopyrimidine derivatives

Highly substituted tetrahydroimidazopyrimidine derivatives with three chiral centers have been synthesized for the first time using an organocatalytic asymmetric domino aza-Michael - Mannich reaction of α,β-unsaturated aldehydes and N-arylidene-1H-imidazo