5270-94-0

Usage

Chemical Properties

Yellow liquid

InChI:InChI=1/C6H8N2O2/c1-9-5-3-6(10-2)8-4-7-5/h3-4H,1-2H3

Upstream product

• 13223-25-1 2-chloro-4,6-dimethoxypyrimidine 
• 75-09-2 dichloromethane 
• 584-08-7 potassium carbonate 
• 2258-42-6 formyl acetic anhydride 
• 1193-21-1 4,6-dichloropyrimidine 
• 124-41-4 sodium methylate 

Downstream Products

• 126327-70-6 (4,6-Dimethoxy-pyrimidin-5-yl)-phenyl-methanol 
• 126327-71-7 (4,6-Dimethoxy-pyrimidin-5-yl)-phenyl-methanone 
• 13566-63-7 5-Methyl-4,6-dimethoxy-pyrimidin 
• 4319-77-1 5-bromo-4,6-dimethoxypyrimidine 
• 491871-36-4 4-[(4,6-dimethoxypyrimidin-2-yl)oxy]benzaldehyde 

Relevant academic research and scientific papers

Triazolopyrimidine cannabinoid receptor 1 antagonists

The present application describes compounds according to both Formulas I and II, pharmaceutical compositions comprising at least one compound according to either Formula I or II and optionally one or more additional therapeutic agents, and methods of treatment using the compounds according to Formulas I and II both alone and in combination with one or more additional therapeutic agents. The compounds have the following general formulas: including all prodrugs, solvates, pharmaceutically acceptable salts and stereoisomers, wherein R1, R2, R3, R4 and R5 are described herein.

Carbonylation of 2-chloro-4,6-dimethoxypyrimidine and 2-(chloromethyl)- 4,6-dimethoxypyrimidine

The preparation of pyrimidine-2-carboxylates and 2-pyrimidineacetates by alkoxycarbonylation of respectively 2-chloropyrimidine and 2- (chloromethyl)pyrimidine with carbon monoxide in the presence of palladium acetate and 1,1'-bis(diphenylphosphino)ferroc

Process for the production of 4,6-dialkoxypyrimidines

A process for the production of 4,6-dialkoxypyrimidines of the general formula: STR1 A propanediimidate of the general formula: STR2 is converted with an anhydride of the general formula: STR3 to provide the product.