56032-35-0

Usage

Uses

Used in Pharmaceutical Industry:
4-chloro-6-methoxy-2-(methylthio)-5-nitropyrimidine serves as an intermediate in the synthesis of pharmaceuticals. Its unique chemical structure allows it to be a key component in the development of new drugs, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 4-chloro-6-methoxy-2-(methylthio)-5-nitropyrimidine is utilized as an intermediate in the production of various agrochemicals. Its role in this industry is crucial for the synthesis of compounds that can help improve crop protection and yield.
Used in Organic Synthesis:
4-chloro-6-methoxy-2-(methylthio)-5-nitropyrimidine acts as a building block in organic synthesis. Its versatile structure makes it suitable for the creation of a wide range of organic compounds, which can be applied across different fields.
Used in Chemical Research:
4-chloro-6-methoxy-2-(methylthio)-5-nitropyrimidine is also used in chemical research, where its properties and reactions are studied to gain insights into new chemical processes and the development of innovative materials. Its high purity and stability make it an ideal candidate for such studies.

Upstream product

• 1979-96-0 4,6-dichloro-2-(methylthio)-5-nitropyrimidine 
• 67-56-1 methanol 
• 124-41-4 sodium methylate 

Relevant academic research and scientific papers

MTOR INHIBITOR COMPOUNDS

The invention relates to novel mTOR inhibitor compounds. The invention is characterized in that the mTOR inhibitor compounds have general formula (I). The invention also relates to compositions comprising said mTOR inhibitor compounds, methods for produci

Reactivity of the pyrimidine nitrogen atom toward an acetal moiety: Formation of 3-ethoxy-2,3-dihydroimidazo[1,2-c ]pyrimidines by intramolecular cyclization of n -(2,2-diethoxyethyl)pyrimidine-4-amines

A new protocol was developed for the synthesis of 2,3-dihydroimidazo[1,2-c] pyrimidines, based on an intramolecular reaction between a pyrimidine nitrogen atom and an acetal moiety in the presence of boron trifluoride etherate. The method was expanded to permit the synthesis of the triheterocyclic imidazo[1,2-c]pyrazolo[4,3-e]pyrimidine system.

Thiazolo-pyrimidine/pyridine urea derivatives

There are presented compounds of the formula or a pharmaceutically acceptable salt thereof, which are active adenosine A2B receptor antagonists and useful in the treatment of diabetes, diabetic retinopathy, asthma and diarrhea.

2,4,5,6-Tetrasubstituted pyrimidines and salts thereof

Compounds of the formula SPC1 Wherein R1 is alkoxy of 1 to 3 carbon atoms, morpholino, thiomorpholino, 1-oxido-thiomorpholino, 1,1-dioxido-thiomorpholino, or EQU1 where A is hydrogen, alkanoyl of 1 to 4 carbon atoms, alkenoyl of 2 to 4 carbon atoms, methoxy-(alkanoyl of 1 to 4 carbon atoms), carboxyl-(alkanoyl of 1 to 4 carbon atoms), acetyl-(alkanoyl of 1 to 4 carbon atoms), methoxy-(alkenoyl of 2 to 4 carbon atoms), carboxyl-(alkenoyl of 2 to 4 carbon atoms), acetyl-(alkenoyl of 2 to 4 carbon atoms), aminocarbonyl, mono(alkyl of 1 to 4 carbon atoms)-aminocarbonyl, di-(alkyl of 1 to 4 carbon atoms)-aminocarbonyl, methoxymethylaminocarbonyl, pyridinoyl, salicyloyl, furanoyl, or (alkyl of 1 to 3 carbon atoms)-sulfonyl, R2 is morpholino, thiomorpholino, 1-oxido-thiomorpholino, 1,1-dioxido-thiomorpholino, piperazino or N'-[acetyl-(alkanoyl of 1 to 3 arbon atoms)]-piperazino, R3 is hydrogen, chlorine, bromine, nitro, cyano, formyl, acetyl or carbalkoxy of 2 to 4 carbon atoms, and R4 is hydrogen, chlorine, bromine, cyano, carbalkoxy of 2 to 4 carbon atoms, alkyl of 1 to 6 carbon atoms, mono(carbalkoxy of 2 to 4 carbon atoms)-alkyl of 1 to 6 carbon atoms, di(carbalkoxy of 2 to 4 carbon atoms)-alkyl of 1 to 6 carbon atoms, hydroxyl, allyloxy, alkoxy of 1 to 6 carbon atoms, mercapto, allylmercapto, (alkyl of 1 to 6 carbon atoms)-mercapto, 1-oxidothiomorpholino, or where B is hydrogen, alkyl of 1 to 3 carbon atoms, cyclohexyl, phenyl, chloro-phenyl, carboxy-phenyl, carbomethoxy-phenyl or pyridyl, And non-toxic, pharmacologically acceptable acid addition salts thereof; the compounds as well as the salts are useful as antithrombotics.