Unlocking Mirabegron Synthesis: The Role of (1R)-2-[2-(4-nitrophenyl)ethylamino]-1-phenylethanol

A critical pharmaceutical intermediate for overactive bladder treatments, essential for efficient API manufacturing.

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Advantages of Using This Intermediate

Streamlined Synthesis

Utilizing this compound as a key building block significantly simplifies the pharmaceutical synthesis of Mirabegron, reducing reaction steps and improving overall yield. This is a crucial aspect of API manufacturing.

Enantiomeric Purity

The compound's inherent chirality is essential for producing the correct enantiomer of Mirabegron, a requirement for its therapeutic efficacy and safety in treating overactive bladder. This contributes to precise chiral synthesis of APIs.

Quality Assurance

With a high assay purity of ≥98.0%, it meets stringent pharmaceutical standards, ensuring the quality and consistency of the final drug product, a hallmark of reliable specialty chemical intermediates for pharma.

Key Applications

Mirabegron Manufacturing

This compound is directly used in the multi-step synthesis of Mirabegron, a drug targeting the beta-3 adrenergic receptor for overactive bladder. It's a cornerstone in pharmaceutical intermediates production.

API Development

Its utility extends to the broader field of Active Pharmaceutical Ingredient (API) development, serving as a versatile intermediate for other complex molecules requiring similar structural motifs. This highlights its value in API manufacturing.

Chiral Chemistry Research

Researchers in chiral chemistry utilize this compound to explore novel synthetic routes and methodologies for creating enantiomerically pure pharmaceuticals. It's a prime example for chiral synthesis of APIs.

Organic Synthesis

Beyond Mirabegron, it serves as a valuable reagent in various organic synthesis projects where the specific arrangement of its functional groups is beneficial for creating target molecules. This is central to organic synthesis pathways.

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