397247-79-9

Basic information

• Product Name: 6,7-dihydro-6-(2,3,5,6-tetrahydropyran-2-yl)oxy-4-methoxy-9-tosylaminopyrido[3',2':4,5]pyrrolo[1,2-c]pyrimidine
• Synonyms: 6,7-dihydro-6-(2,3,5,6-tetrahydropyran-2-yl)oxy-4-methoxy-9-tosylaminopyrido[3',2':4,5]pyrrolo[1,2-c]pyrimidine
• CAS NO: 397247-79-9
• Molecular Weight: 470.549
• Mol File: 397247-79-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 6,7-dihydro-6-(2,3,5,6-tetrahydropyran-2-yl)oxy-4-methoxy-9-tosylaminopyrido[3',2':4,5]pyrrolo[1,2-c]pyrimidine(CAS DataBase Reference)
• NIST Chemistry Reference: 6,7-dihydro-6-(2,3,5,6-tetrahydropyran-2-yl)oxy-4-methoxy-9-tosylaminopyrido[3',2':4,5]pyrrolo[1,2-c]pyrimidine(397247-79-9)
• EPA Substance Registry System: 6,7-dihydro-6-(2,3,5,6-tetrahydropyran-2-yl)oxy-4-methoxy-9-tosylaminopyrido[3',2':4,5]pyrrolo[1,2-c]pyrimidine(397247-79-9)

Safety Data

• Hazardous Substances Data: 397247-79-9(Hazardous Substances Data)

Upstream product

• 110-87-2 3,4-dihydro-2H-pyran 
• 1886-67-5 N-tosyldichloromethanimine 
• 397247-69-7 2-[2-amino-1-(2,3,5,6-tetrahydropyran-2-yl)oxyethyl]-4-methoxy-7-azaindole 
• 397247-67-5 4-methoxy-2-[2-phthalimido-1-(2,3,5,6-tetrahydropyran-2-yl)oxyethyl]-7-azaindole 
• 397247-65-3 2-(1-hydroxy-2-phthalimidoethyl)-4-methoxy-7-azaindole 
• 122379-63-9 4-methoxy-1H-pyrrolo<2,3-b>pyridine 

Downstream Products

• 397247-85-7 4-methoxy-9-tosylaminopyrido[3',2':4,5]pyrrolo[1,2-c]pyrimidine 
• 397247-88-0 5-iodo-4-methoxy-9-tosylaminopyrido[3',2':4,5]pyrrolo[1,2-c]pyrimidine 
• 397247-90-4 5-(2-aminopyrimidin-4-yl)-4-hydroxy-9-tosylaminopyrido[3',2':4,5]pyrrolo[1,2-c]pyrimidine 
• 397247-89-1 5-(2-acetylaminopyrimidin-4-yl)-4-methoxy-9-tosylaminopyrido[3',2':4,5]pyrrolo[1,2-c]pyrimidine 
• 397247-82-4 6,7-dihydro-6-hydroxy-4-methoxy-9-tosylaminopyrido[3',2':4,5]pyrrolo[1,2-c]pyrimidine 

Relevant articles and documents

Synthesis of variolin B

The total synthesis of variolin B from 4-methoxy-7-azaindole is described. The preparation of the protected amino derivative 10 and a coupling reaction of the iodo derivative 12 with 2-acetylamino-4-trimethylstannylpyrimidine are the key steps of the sequ