69696-38-4

Upstream product

• 2814-20-2 2-isopropyl-6-methyl-4-pyrimidinol 
• 2814-20-2 2-Isopropyl-6-methyl-4(3H)-pyrimidone 

Downstream Products

• 1040741-71-6 2-[allyl-(5-iodo-2-isopropyl-6-methyl-pyrimidin-4-yl)-amino]-4-methylpentanoic acid cyclohexylamide 
• 1040741-70-5 2-[allyl-(5-iodo-2-isopropyl-6-methyl-pyrimidin-4-yl)-amino]-4-methylpentanoic acid 4-methoxy-benzylamide 
• 1040741-72-7 2-(allyl(5-iodo-2-isopropyl-6-methylpyrimidin-4-yl)amino)-N-(4-chlorobenzyl)butanamide 
• 1040741-85-2 2-(2-isopropyl-4,5-dimethyl-pyrrolo[2,3-d]pyrimidin-7-yl)-4-methyl-pentanoic acid 4-chloro-benzylamide 
• 1236282-88-4 N-cyclohexyl-2-[(5-iodo-2-isopropyl-6-methylpyrimidin-4-yl)-(2-methoxyethyl)-amino]-acetamide 
• 1236282-86-2 N-tert-butyl-2-[(4-chlorobenzyl)-(5-iodo-2-isopropyl-6-methylpyrimidin-4-yl)-amino]-acetamide 
• 1236282-83-9 2-[butyl-(5-iodo-2-isopropyl-6-methylpyrimidin-4-yl)-amino]-N-(4-methoxybenzyl)-acetamide 
• 1236282-84-0 N-(4-chlorobenzyl)-2-[(4-chlorobenzyl)-(5-iodo-2-isopropyl-6-methylpyrimidin-4-yl)-amino]-acetamide 
• 1236282-79-3 2-[(4-chlorobenzyl)-(5-iodo-2-isopropyl-6-methylpyrimidin-4-yl)-amino]-N-cyclohexyl-2-(4-fluorophenyl)-acetamide 
• 1236282-81-7 2-[(4-chlorobenzyl)-(5-iodo-2-isopropyl-6-methylpyrimidin-4-yl)-amino]-2-(4-fluorophenyl)-N-(4-methoxybenzyl)-acetamide 
• 1236282-73-7 N-(4-chlorobenzyl)-2-[(4-chlorobenzyl)-(5-iodo-2-isopropyl-6-methylpyrimidin-4-yl)-amino]-2-(4-fluorophenyl)-acetamide 
• 1236282-77-1 2-[butyl-(5-iodo-2-isopropyl-6-methylpyrimidin-4-yl)-amino]-N-(4-chlorobenzyl)-2-phenylacetamide 
• 1272662-65-3 N-methyl-N-(5-methylfuran-2-ylmethyl)-5-iodo-2-isopropyl-6-methylpyrimidin-4-amine 
• 1272663-07-6 N-(4-chlorobenzyl)-2-[furan-2-ylmethyl-(5-iodo-2-isopropyl-6-methylpyrimidin-4-yl)-amino]-acetamide 

Relevant academic research and scientific papers

Palladium-catalyzed ring opening of aminocyclopropyl Ugi adducts

The ring opening of aminocyclopropanes triggered by activation with an intramolecular arylpalladium(II) iodide complex is an interesting strategy for the synthesis of nitrogen heterocycles and a valuable Ugi postcondensation-type transformation. Six- and

Palladium catalyzed ring opening of furans as a route to α,β-unsaturated aldehydes

Furans may be ring opened via pallado-catalyzed reactions leading to α,β-unsaturated aldehydes and ketones tethered to indole and isoquinoline moieties. Besides their synthetic interest, these fragmentations bring interesting elements into the discussion