115492-22-3

Upstream product

• 126898-87-1 5-(1-iodo-2-p-toluoylvinyl)uracil 
• 874-60-2 4-methyl-benzoyl chloride 
• 122352-88-9 2,4-dimethoxy-5-(3-tetrahydropyran-2-yloxyprop-1-ynyl)-pyrimidine 
• 115492-12-1 3-(2,4-dimethoxypyrimidin-5-yl)-1-(p-tolyl)-2-propyn-1-one 
• 122352-89-0 5-(2-hydroxymethylethynyl)-2,4-dimethoxypyrimidine 
• 106-38-7 para-bromotoluene 
• 115492-19-8 5-((Z)-1-Iodo-3-oxo-3-p-tolyl-propenyl)-1H-pyrimidine-2,4-dione 
• 122353-07-5 5-(1-chloro-2-p-toluoylvinyl)uracil 
• 83355-89-9 2,4-Dimethoxy-5-trimethylsilanylethynyl-pyrimidine 

Relevant academic research and scientific papers

Synthesis of Dimethoxypyrimidines and Uracils with Novel C-5 Substituents

5-Iodo-2,4,-dimethoxypyrimidine 1 on treatment with copper(I) 3-tetrahydropyran-2-yloxyprop-1-ynide was converted into 2,4-dimethoxy-5-(3-tetrahydropyran-2-yloxyprop-1-ynyl)pyrimidine 2 which on treatment with toluene-p-sulphonic acid in methanol led to 5

Synthesis and Biological Activities of Novel 5-(2-Acylethynyl)uracils

5-(2-Acylethynyl)-2,4-dimethoxypyrimidines (3-6) were synthesized in excellent yields from 2,4-dimethoxy-5-pyrimidine (2) by treatment with acid chlorides in the presence of anhydrous aluminum chloride.Compounds 3-6 were deblock

A General Procedure for the Synthesis of Dimethoxypyrimidines and Uracils with Highly Functionalised C-5 Substituents

A versatile method for the synthesis of 5--2,4-dimethoxypyrimidines (5)-(13), 5-(2-acyl-ethynyl)2,4-dimethoxypyrimidines (14)-(22), 5-(2-acyl-chlorovinyl)uracils (23)-(27) and 5-(2-acylethynyl)uracils (28)-(30) is d