388573-33-9

Basic information

• Product Name: 4-methoxy-9-(4-methoxybenzylamino)-5-[2-(4-methoxybenzylamino)pyrimidin-4-yl]pyrido[3',2':4,5]pyrrolo[1,2-c]pyrimidine
• Synonyms: 4-methoxy-9-(4-methoxybenzylamino)-5-[2-(4-methoxybenzylamino)pyrimidin-4-yl]pyrido[3',2':4,5]pyrrolo[1,2-c]pyrimidine
• CAS NO: 388573-33-9
• Molecular Weight: 547.616
• Mol File: 388573-33-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 4-methoxy-9-(4-methoxybenzylamino)-5-[2-(4-methoxybenzylamino)pyrimidin-4-yl]pyrido[3',2':4,5]pyrrolo[1,2-c]pyrimidine(CAS DataBase Reference)
• NIST Chemistry Reference: 4-methoxy-9-(4-methoxybenzylamino)-5-[2-(4-methoxybenzylamino)pyrimidin-4-yl]pyrido[3',2':4,5]pyrrolo[1,2-c]pyrimidine(388573-33-9)
• EPA Substance Registry System: 4-methoxy-9-(4-methoxybenzylamino)-5-[2-(4-methoxybenzylamino)pyrimidin-4-yl]pyrido[3',2':4,5]pyrrolo[1,2-c]pyrimidine(388573-33-9)

Safety Data

• Hazardous Substances Data: 388573-33-9(Hazardous Substances Data)

Upstream product

• 388573-29-3 bis-[2-(methylsulfayl)pyrimidin-4-yl]methanone 
• 388573-30-6 (2-chloro-4-methoxypyridin-3-yl)-bis-[2-(methylsulfayl)pyrimidin-4-yl]methanol 
• 388573-31-7 4-methoxy-9-(methylsulfanyl)-5-[2-(methylsulfanyl)pyrimidin-4-yl]pyrido[3',2':4,5]pyrrolo[1,2-c]pyrimidine 
• 52545-13-8 4-methoxypyridin-2(1H)-one 
• 17228-69-2 2-chloro-4-methoxy-pyridine 
• 1124-33-0 4-nitraminopyridine N-oxide 
• 1122-96-9 4-methoxypyridine N-oxide 
• 864229-50-5 (2-chloro-4-methoxypyridin-3-yl)-bis-[2-(methylsulfayl)pyrimidin-4-yl]methyl acetate 
• 864229-51-6 ethyl 2-chloro-4-methoxypyridine-3-carboxylate 
• 2393-23-9 4-methoxy-benzylamine 
• 388573-32-8 9-Methanesulfinyl-5-(2-methanesulfinyl-pyrimidin-4-yl)-4-methoxy-pyrido[3',2':4,5]pyrrolo[1,2-c]pyrimidine 

Downstream Products

• 388573-34-0 4-hydroxy-9-(4-methoxybenzylamino)-5-[2-(4-methoxybenzylamino)pyrimidin-4-yl]pyrido[3',2':4,5]pyrrolo[1,2-c]pyrimidine 

Relevant articles and documents

Concise total syntheses of variolin B and deoxyvariolin B

The total synthesis of the marine alkaloid variolin B has been achieved in 8 steps and 17% overall yield, starting from commercially available 4-chloro-2-methylthiopyrimidine. The key reaction involves the tandem deoxygenation and cyclization of a triarylmethanol using a combination of triethylsilane and trifluoroacetic acid. In addition, the deoxygenated analogue was prepared in 6 steps and 23% overall yield, starting from the same starting material.