102064-38-0

Basic information

• Product Name: Pyrido[3,2-e]pyrrolo[1,2-a]pyrazine, 5,6-dihydro-6,6-dimethyl- (9CI)
• Synonyms: Pyrido[3,2-e]pyrrolo[1,2-a]pyrazine, 5,6-dihydro-6,6-dimethyl- (9CI)
• CAS NO: 102064-38-0
• Molecular Formula: C12H13N3
• Molecular Weight: 199.25172
• Product Categories: PYRIDINE
• Mol File: 102064-38-0.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Pyrido[3,2-e]pyrrolo[1,2-a]pyrazine, 5,6-dihydro-6,6-dimethyl- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Pyrido[3,2-e]pyrrolo[1,2-a]pyrazine, 5,6-dihydro-6,6-dimethyl- (9CI)(102064-38-0)
• EPA Substance Registry System: Pyrido[3,2-e]pyrrolo[1,2-a]pyrazine, 5,6-dihydro-6,6-dimethyl- (9CI)(102064-38-0)

Safety Data

• Hazardous Substances Data: 102064-38-0(Hazardous Substances Data)

Upstream product

• 102064-39-1 chlorhydrate de dihydro-5,6 dimethyl-6,6 pyrido<3,2-e>pyrrolo<1,2-a>pyrazine 
• 4214-75-9 2-amino-3-nitropyridine 
• 102064-27-7 3-nitro-2-(1H-pyrrol-1-yl)pyridine 
• 102064-33-5 chlorure de (pyrrolyl-1)-2 pyridyl ammonium-3 
• 102064-32-4 2-(1H-pyrrol-1-yl)-3-aminopyridine 
• 67-63-0 isopropyl alcohol 

Relevant articles and documents

One-pot synthesis of pyrrolo[1,2-a]quinoxaline derivatives via iron-promoted aryl nitro reduction and aerobic oxidation of alcohols

Here, we describe a new one-pot method to synthesize 4,7-substituted pyrrolo[1,2-a]quinoxalines and related heterocyles through a cascade of redox reactions/imine formation/intramolecular cyclization. This procedure tolerates readily available substituted 1-(2-nitrophenyl)pyrrole derivatives and aliphatic or benzylic alcohols as starting materials using iron powder and acidic conditions. This is the first example of constructing N-heterocycles via iron-mediated aryl nitro reduction and aerobic oxidation of alcohols in one pot.

Pyridopyrrolopyrazines

Pyridopyrrolopyrazines are prepared by intramolecular cyclization of (pyrrolyl-1)-2 pyridine derivatives.Proton magnetic resonance (1H-HMR) are studied.