1094100-06-7 | (3R,5R,E)-7-(4-(4-Fluorophenyl)-6-isopropyl-2-(N-methylmethylsulfonamido)pyrimidin-5-yl)-3,5-dihydroxyhept-6-enoic acid

Availability
Typically In Stock

Description

• Catalog Number: AE14341
• Chemical Name: (3R,5R,E)-7-(4-(4-Fluorophenyl)-6-isopropyl-2-(N-methylmethylsulfonamido)pyrimidin-5-yl)-3,5-dihydroxyhept-6-enoic acid
• CAS Number: 1094100-06-7
• Molecular Formula: C22H28FN3O6S
• Molecular Weight: 481.53762319999987
• MDL Number: MFCD23115836
• SMILES: O[C@H](C[C@H](CC(=O)O)O)C=Cc1c(nc(nc1c1ccc(cc1)F)N(S(=O)(=O)C)C)C(C)C

Upstream Synthesis Route

The compound (3R,5R,6E)-7-[4-(4-fluorophenyl)-6-(1-methylethyl)-2-[methyl(methylsulfonyl)amino]-5-pyrimidinyl]-3,5-dihydroxy-6-heptenoic acid, commonly referred to as $name$, plays a crucial role in chemical synthesis as a key intermediate in the production of pharmaceutical compounds. Its unique structure and functional groups make it a valuable building block for the synthesis of various drug candidates and active pharmaceutical ingredients.$name$ is particularly versatile in chemical reactions due to the presence of multiple reactive sites, including hydroxy, amino, and fluorophenyl groups. These functional groups allow for the introduction of additional substitutions and modifications to fine-tune the properties and biological activities of the final compounds. By utilizing $name$ in synthesis, chemists can access a wide range of derivatives with enhanced pharmacological profiles and improved drug-like characteristics.In organic chemistry, $name$ can serve as a starting material for the construction of complex molecular scaffolds through diverse synthetic methodologies such as coupling reactions, halogenation, and functional group transformations. This compound's strategic placement of substituents enables precise control over stereochemistry and regioselectivity during chemical manipulations, facilitating the creation of stereochemically defined and structurally intricate molecules.Overall, the application of (3R,5R,6E)-7-[4-(4-fluorophenyl)-6-(1-methylethyl)-2-[methyl(methylsulfonyl)amino]-5-pyrimidinyl]-3,5-dihydroxy-6-heptenoic acid in chemical synthesis empowers chemists to access novel drug candidates and therapeutic agents with improved potency, selectivity, and pharmacokinetic properties. By leveraging the synthetic capabilities of $name$, researchers can accelerate the discovery and development of innovative pharmaceuticals to address unmet medical needs and advance the field of medicinal chemistry.