139962-70-2

Basic information

• Product Name: 1H-Pyrrolo[2,3-b]pyridine, 3-methyl-2-phenyl-
• CAS NO: 139962-70-2
• Molecular Formula: C14H12N2
• Molecular Weight: 208.263
• Mol File: 139962-70-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1H-Pyrrolo[2,3-b]pyridine, 3-methyl-2-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrrolo[2,3-b]pyridine, 3-methyl-2-phenyl-(139962-70-2)
• EPA Substance Registry System: 1H-Pyrrolo[2,3-b]pyridine, 3-methyl-2-phenyl-(139962-70-2)

Safety Data

• Hazardous Substances Data: 139962-70-2(Hazardous Substances Data)

Upstream product

• 536-78-7 3-ethylpyridine 
• 100-47-0 benzonitrile 
• 1603-40-3 3-methylpyridin-2-ylamine 
• 161987-58-2 1-(2-pivaloylaminopyridin-3-yl)ethanone 
• 86847-59-8 2-(pivaloylamino)pyridine 
• 945607-91-0 C₈H₈Cl₂N₂ 
• 945607-65-8 C₁₃H₁₆Cl₂N₂O 
• 945607-79-4 [3-(2,2-dichloro-1-methylvinyl)-pyridin-2-yl]-carbamic acid tert-butyl ester 
• 98-80-6 phenylboronic acid 
• 149489-03-2 tert-butyl (3-ethylpyridin-2-yl)carbamate 
• 138343-75-6 tert-butyl (3-methylpyridin-2-yl)carbamate 

Downstream Products

• 145934-33-4 3-Methyl-2-phenyl-7-phenacyl pyrrolo[2,3-b]pyridine 

Relevant articles and documents

2-SUBSTITUTED AZAIN DOLES AND 2 SUBSTITUTED THIENOPYRROLES, THEIR PRECURSORS AND NOVEL PROCESSES FOR THE PREPARATION THEREOF

The present invention relates generally to processes for the chemical synthesis of azaindole and thienopyrrole compounds, in particular azaindole and thienopyrrole compounds that are substituted at the 2-position of the azaindole or thienopyrrole ring, an

A convenient method for the preparation of 5-, 6- and 7-azaindoles and their derivatives

The directed ortho lithiation of 2-tert-butoxycarbonylamino-3-methylpyridine (6a) has provided a convenient method for the preparation of 1H-pyrrolo[2,3-b]pyridine (4a, 7-azaindole). This procedure has been used to prepare a range of 3-substituted 2-tert-butoxycarbonylaminopyridines 6, 2- and 3-substituted and 2,3-disubstituted 1H-pyrrolo[2,3-b]pyridines 4 and shown to be of value in the preparation of 1H-pyrrolo[3,2-c]pyridine (15, 5-azaindole) and 1H-pyrrolo[2,3-c]pyridine (18, 6-azaindole) and derivatives.

Reactions of β-(lithiomethyl)azines with nitriles as a route to pyrrolo-pyridines, - quinolines, -pyrazines, - quinoxalines and -pyrimidines

Deprotonation of 3-methylazines, followed by reaction with benzonitile, gives an intermediate which, on treatment with additional strong base, cyclises to give 2-phenyl[1H]-pyrrolo[2,3-b]pyridine. The application of this type of reaction to a variety of n