129006-32-2

Upstream product

• 62-53-3 aniline 
• 13162-27-1 5-amino-2,4-dichloro-6-methylpyrimidine 
• 129006-31-1 5-amino-4-anilino-2-chloro-6-methylpyrimidine 
• 122-51-0 orthoformic acid triethyl ester 

Downstream Products

• 140421-38-1 6-methyl-2-methoxy-9-phenyl-9H-purine 
• 140421-45-0 6-methyl-2-(methylthio)-9-phenyl-9H-purine 
• 129006-36-6 6-Methyl-9-phenyl-9H-purine-2-carbonitrile 
• 129006-44-6 (6-Methyl-8,9-diphenyl-9H-purin-2-yl)-phenyl-methanone 
• 129006-42-4 1-(6-Methyl-9-phenyl-9H-purin-2-yl)-propan-1-one 
• 129006-41-3 1-(6-Methyl-9-phenyl-9H-purin-2-yl)-ethanone 
• 140421-41-6 2-(2-Methoxy-9-phenyl-9H-purin-6-yl)-1-phenyl-ethanone 
• 140421-40-5 2-Methoxy-9-phenyl-6-((E)-styryl)-9H-purine 
• 140421-34-7 9-phenyl-6-styryl-9H-purine 
• 140421-43-8 2-Methoxy-9-phenyl-9H-purine-6-carbaldehyde 
• 140421-36-9 9-Phenyl-9H-purine-6-carbaldehyde 
• 140421-33-6 6-methyl-9-phenyl-9H-purine 
• 70386-35-5 phenyl (9-phenyl-9H-purin-6-yl)methyl ketone 

Relevant academic research and scientific papers

Purines. X. Reactivities of methyl groups on 9-phenylpurines: Condensation with an aldehyde or an ester, and oxidation with selenium dioxide

The condensation of a methyl group at the 6- or 8-position on the 9H-purine ring with benzaldehyde and ethyl benzoate in the presence of sodium hydride occurred to give the styryl- (4a, b) and phenacyl-9H-purines (5a, b and 6a,b). Conversion of the methyl

PURINES. IX. REACTION OF 9-PHENYL-9H-PURINE-2-CARBONITRILES WITH GRIGNARD REAGENTS

The palladium-catalyzed cross-coupling reaction of 2- and 6-chloro-9-phenyl-9H-purines with potassium cyanide proceeded to give 9-phenyl-9H-purine-2- (3a-c) and -6-carbonitriles (4a-c).The conversion of the cyano group at the 2-position into the correspon