N-Methyl-N-((3R,4R)-4-methylpiperidin-3-yl)-7H-pyrrolo2,3-dpyrimidin-4-amine丨CAS 477600-74-1

N-Methyl-N-((3R,4R)-4-methylpiperidin-3-yl)-7H-pyrrolo2,3-dpyrimidin-4-amine丨CAS 477600-74-1
Product Introduction:
Catalog No.: SS143384
CAS No.: 477600-74-1
Assay: 98.0% min.
Product Name: N-Methyl-N-((3R,4R)-4-methylpiperidin-3-yl)-7H-pyrrolo2,3-dpyrimidin-4-amine
Molecular Formula: C13H19N5
Molecular Weight: 245.32
Send Inquiry
Technical Parameters
Description

Hangzhou Leap Chem Co., Ltd. is one of the most professional manufacturers and suppliers of n-methyl-n-((3r,4r)-4-methylpiperidin-3-yl)-7h-pyrrolo2,3-dpyrimidin-4-amine丨cas 477600-74-1 in China. Welcome to wholesale bulk high quality chemical products at competitive price from our factory. If you have any enquiry about custom service, please feel free to email us.

 

Specifications

 

Appearance White to off-white or greyish powder
Assay 98.0% min.
Loss on drying 1.0% max.
Any unknown impurity 0.5% max.
Total impurities 1.0% max.

 

 

 

Applications

 

This compound is primarily used as a key intermediate in the synthesis of bioactive molecules, particularly in antiviral, anticancer, and kinase inhibitor research. Its heterocyclic pyrrolopyrimidine scaffold is common in drug candidates targeting protein kinases and other cellular enzymes, making it useful for the development of targeted therapies. The chiral piperidine moiety allows for stereoselective interactions with biological targets, enhancing efficacy and specificity. It is also employed in medicinal chemistry for structure–activity relationship (SAR) studies, helping chemists optimize pharmacological properties of drug candidates. Additionally, it may serve as a building block in the synthesis of complex nitrogen-containing heterocycles and analogues in pharmaceutical research and development.

 

Benefits

 

The main benefits of this compound lie in its dual functionality: the nitrogen-rich heterocyclic core enables diverse chemical transformations, while the chiral piperidine provides stereochemical control for selective biological activity. Its stability under typical synthetic conditions allows safe handling and incorporation into multi-step syntheses. The presence of reactive amino groups facilitates further derivatization, enabling the design of derivatives with improved solubility, potency, or selectivity. Its well-defined stereochemistry supports the development of enantiomerically pure drug candidates, which is critical in modern medicinal chemistry.

 

Conclusion

 

N-Methyl-N-((3R,4R)-4-methylpiperidin-3-yl)-7H-pyrrolo[2,3-d]pyrimidin-4-amine is a versatile heterocyclic intermediate widely used in pharmaceutical synthesis and medicinal chemistry. Its combination of a pyrrolopyrimidine core and chiral piperidine allows for the creation of bioactive molecules with high specificity and potency. As demand for novel therapeutics and targeted drug candidates grows, this compound remains an important building block in modern drug discovery and development.

 

Send Inquiry
Beyond Your Expectation
From Science to Life with LEAPChem
contact us