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Suzuki Coupling Reaction

Enabling efficient, scalable Suzuki coupling with advanced palladium catalysts and scalable protocols

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What is Suzuki Coupling Reaction?

Suzuki coupling is a palladium-catalyzed cross-coupling reaction between organoboron compounds and halides, facilitating the formation of carbon-carbon bonds. This versatile reaction is essential for synthesizing complex organic molecules in pharmaceuticals, agrochemicals, and other specialty chemicals.

Cyanation reaction mechanism

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EU GMP Certification Logo
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WHO GMP Certification Logo
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GMP Certification Logo
Kosher Certification Logo
FDA Approved Certification Logo
EU GMP Certification Logo
GFSI Certification Logo
WHO GMP Certification Logo
US FDA Logo
PMDA (Pharmaceuticals and Medical Devices Agency) Logo
FSSAI Certification Logo
GMP Certification Logo
Kosher Certification Logo
FDA Approved Certification Logo
EU GMP Certification Logo
GFSI Certification Logo
WHO GMP Certification Logo
US FDA Logo
PMDA (Pharmaceuticals and Medical Devices Agency) Logo
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GMP Certification Logo
Kosher Certification Logo
FDA Approved Certification Logo
EU GMP Certification Logo
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Applications of Suzuki Coupling in key industries

Pharmaceuticals

Enables the synthesis of advanced APIs and intermediates, particularly for oncology and antiviral drugs.

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Pharmaceuticals

Agrochemicals

Used to create active ingredients in herbicides, fungicides, and insecticides with improved efficiency.

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Agrochemicals

Industrial Chemicals

Facilitates the development of advanced materials, including polymers and chemical precursors.

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Industrial Chemicals

Suzuki Couplings in the Synthesis of Losartan

The Suzuki-Miyaura coupling reaction is a key step in the synthesis of Losartan, an angiotensin II receptor blocker (ARB) used to treat hypertension. This palladium-catalyzed cross-coupling reaction enables the formation of a biaryl bond, which is essential for the drug's pharmacological activity.

Reaction

Aryl Halide Substrate: 2-Butyl-4-chloro-5-formylimidazole

Boron Reagent: 4-(Boronate)Biphenyl (Boronic acid derivative)

Catalyst: Palladium(0) complex (e.g., Pd(PPh₃)₄)

Base: Potassium carbonate (K₂CO₃) or Sodium hydroxide (NaOH)

Solvent: Tetrahydrofuran (THF) or Aqueous-organic system

2-Butyl-4-chloro-5-formylimidazole+4-(Boronate)BiphenylPd(0),Base,SolventLosartan Intermediate\text{2-Butyl-4-chloro-5-formylimidazole} + \text{4-(Boronate)Biphenyl} \xrightarrow[]{\text{Pd(0)}, \text{Base}, \text{Solvent}} \text{Losartan Intermediate}
2-Butyl-4-chloro-5-formylimidazole+4-(Boronate)BiphenylPd(0),Base,SolventLosartan Intermediate\begin{gathered} \text{2-Butyl-4-chloro-5-formylimidazole} + \text{4-(Boronate)Biphenyl} \\[0.5em] \xrightarrow[]{\text{Pd(0)}, \text{Base}, \text{Solvent}} \\[0.5em] \text{Losartan Intermediate} \end{gathered}

Other Chemistry Capabilities

Cyanation

Cyanation

Cyanation is a chemical process that introduces a cyano group (-CN) in...

Hydrogenation

Hydrogenation

Hydrogenation is a chemical process in which hydrogen (H2) is added to...

Biocatalysis

Biocatalysis

Biocatalysis harnesses the power of enzymes or microorganisms to catal...

Fluorination

Fluorination

Fluorination is a chemical process used to introduce one or more fluor...

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Why Choose Scimplify for Suzuki Coupling Reaction?

Expertise in palladium catalyst optimization for high efficiency and yield

Specialized setups for large-scale cross-coupling reactions under controlled conditions

Comprehensive services and diverse tailored Suzuki coupling protocols for multiple industrial applications

Eco-friendly processes that minimize waste and enable catalyst recycling

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Resources

Webinar

July 4, 2024

Enhancing Innovation in Fragrance Value Chain

👥 Speaker: Vilas Sahasrabuddhey
👤 Host: Hersh Manek - Business Head, Flavors & Fragrances, Scimplify
👤 Co-Host: Nikita Ghode - Senior Manager, Market Intelligence, Scimplify

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May 23, 2023

Key Strategies for Protecting IPR in R&D Outsourcing

👥 Speaker: Dr. T Pavan Kumar
👤 Host: Mr Karthik Kumar - Business Head, Pharmaceuticals, Scimplify