70932-71-7

Upstream product

• 716-43-8 dimethyl homophthalate 
• 124-38-9 carbon dioxide 

Downstream Products

• 1174225-87-6 methyl 2-[1-(hexylamino)-3-methoxy-1,3-dioxopropan-2-yl]benzoate 
• 1174225-91-2 methyl 2-{1-[(benzyloxy)amino]-3-methoxy-1,3-dioxopropan-2-yl}benzoate 
• 1174225-85-4 methyl 2-{1-[(2,4-dimethoxybenzyl)amino]-3-methoxy-1,3-dioxopropan-2-yl}benzoate 
• 1174225-86-5 methyl 2-(1-{[2-(3,4-dimethoxyphenyl)ethyl]amino}-3-methoxy-1,3-dioxopropan-2-yl)benzoate 
• 1174225-88-7 methyl 2-{1-[(3-chlorophenyl)amino]-3-methoxy-1,3-dioxopropan-2-yl}benzoate 
• 1174225-83-2 methyl 2-{1-[(4-fluorobenzyl)amino]-3-methoxy-1,3-dioxopropan-2-yl}benzoate 
• 1174225-89-8 methyl 2-{1-[(2-ethoxy-2-oxoethyl)amino]-3-methoxy-1,3-dioxopropan-2-yl}benzoate 
• 1174226-00-6 methyl 2-(benzyloxy)-1,3-dioxo-1,2,3,4-tetrahydroisoquinoline-4-carboxylate 
• 1436490-25-3 N-(4-fluorobenzyl)-2-methyl-1,3-dioxo-1,2,3,4-tetrahydroisoquinoline-4-carboxamide 
• 1383786-02-4 N-phenyl-2-benzyloxy-1,3-dioxo-1,2,3,4-tetrahydroisoquinoline-4-carboxamide 
• 1383785-88-3 N-(3-chloro-4-methoxyphenyl)-2-benzyloxy-1,3-dioxo-1,2,3,4-tetrahydroisoquinoline-4-carboxamide 
• 1383785-87-2 N-(3-fluorophenyl)-2-benzyloxy-1,3-dioxo-1,2,3,4-tetrahydroisoquinoline-4-carboxamide 
• 1383786-06-8 N-(4-fluorophenyl)-2-benzyloxy-1,3-dioxo-1,2,3,4-tetrahydroisoquinoline-4-carboxamide 
• 1383786-08-0 N-benzyl-2-benzyloxy-1,3-dioxo-1,2,3,4-tetrahydroisoquinoline-4-carboxamide 

Relevant academic research and scientific papers

Synthesis and biological activity of cocaine analogues. 2. 6H-[2]benzopyrano[4,3-c]pyridin-6-ones

1,2,3,4-Tetrahydro-2-methyl-6H-[2] benzopyrano[4,3-c]pyridin-6-one (20) and cis- and trans-1,2,3,4,4a, 10b-hexahydro-2-methyl-6H-2[2]benzopyrano[4,3-c]pyridin-6-one (3a and 3b) were synthesized. The design of 3b was based on the proposal that the active c

2-HYDROXYISOQUINOLINE-1,3(2H,4H)-DIONES AND RELATED COMPOUNDS USEFUL AS HIV REPLICATION INHIBITORS

The present invention relates to compounds and compositions acting as inhibitors of HIV integrase. The compound of the invention is of Formula (I), or a tautomer (I') thereof, or a pharmaceutically acceptable salt, or solvate of said compound or tautomer

Facile synthesis of 4-alkoxycarbonylisoquinoline-1,3-diones and 5-alkoxycarbonyl-2-benzazepine-1,3-diones via a mild alkaline cyclization

(Chemical Equation Presented) A series of 4-methoxycarbonylisoquinoline-1, 3-diones was obtained from homophthalic acid in four steps. The key step was the quantitative and rapid alkaline cyclization of 2-methoxycarbonyl-2-(2- methoxycarbonylphenyl) aceta