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4-(4-Fluorophenyl)-6-Isopropyl-2-[(N-Methyl-N-Methylsulfonyl)Amino]Pyrimidinyl-5-Yl-Formyl

    • Product Name 4-(4-Fluorophenyl)-6-Isopropyl-2-[(N-Methyl-N-Methylsulfonyl)Amino]Pyrimidinyl-5-Yl-Formyl
    • Alias Lefamulin
    • Einecs 694-249-5
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    703297

    Iupac Name 4-(4-Fluorophenyl)-6-isopropyl-2-[(N-methyl-N-methylsulfonyl)amino]pyrimidin-5-ylformyl
    Molecular Formula C18H20FN3O3S
    Molecular Weight 377.44
    Appearance Solid (expected)
    Solubility Likely soluble in DMSO, DMF, and slightly soluble in methanol
    Logp Expected to be moderately lipophilic
    Structure Type Aromatic pyrimidine derivative
    Functional Groups Aldehyde, fluorophenyl, isopropyl, methylsulfonyl, secondary amine
    Smiles CC(C)c1cc(N(S(=O)(=O)C)C)c(C=O)nc1-c2ccc(F)cc2
    Inchi InChI=1S/C18H20FN3O3S/c1-12(2)15-13(10-24)21-18(22(3)26(4,25)23)17(20-15)14-6-8-16(19)9-7-14/h6-9,10,12H,1-4H3

    As an accredited 4-(4-Fluorophenyl)-6-Isopropyl-2-[(N-Methyl-N-Methylsulfonyl)Amino]Pyrimidinyl-5-Yl-Formyl factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100 mg of `4-(4-Fluorophenyl)-6-Isopropyl-2-[(N-Methyl-N-Methylsulfonyl)Amino]Pyrimidinyl-5-Yl-Formyl`, sealed in amber glass vial with tamper-proof cap.
    Shipping This chemical is shipped in a tightly sealed, inert-container, protected from light and moisture. It is handled under ambient temperature and standard safety precautions for organic compounds. Transport complies with all relevant local and international chemical regulations. Accompanying documentation includes safety data sheets and labeling in accordance with GHS/CLP guidelines.
    Storage Store **4-(4-Fluorophenyl)-6-Isopropyl-2-[(N-Methyl-N-methylsulfonyl)amino]pyrimidinyl-5-yl-formyl** in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible substances, such as strong oxidizers. Ensure storage in a dedicated chemical cabinet, with appropriate labeling and access restricted to trained personnel. Follow all safety and local environmental regulations.
    Application of 4-(4-Fluorophenyl)-6-Isopropyl-2-[(N-Methyl-N-Methylsulfonyl)Amino]Pyrimidinyl-5-Yl-Formyl

    Applications of 4-(4-Fluorophenyl)-6-Isopropyl-2-[(N-Methyl-N-Methylsulfonyl)Amino]Pyrimidinyl-5-Yl-Formyl in Industrial Manufacturing

    As the direct manufacturer, we deliver 4-(4-Fluorophenyl)-6-Isopropyl-2-[(N-Methyl-N-Methylsulfonyl)Amino]Pyrimidinyl-5-Yl-Formyl to specialized global markets where precise outcomes and fully documented compliance are essential. Downstream partners leverage its advanced molecular design for high-value product synthesis, relying on stable supply and technical onboarding for integration into established pipelines. Below, we outline authentic industrial fields, production parameters, and typical compliance frameworks.

    1. Active Pharmaceutical Ingredient Synthesis for Cardiovascular Drugs

    Pharmaceutical companies employ this compound as a key intermediate in the multi-step production of selective angiotensin II receptor antagonists. Its inclusion enables the architectural buildup of pyrimidine-based structures with targeted affinity profiles. Production managers use this material during key condensation phases, ensuring high selectivity and low impurity levels. The resulting APIs are processed further for tablet, capsule, and injectable forms. Real-world compliance requirements and exact usage ratios guide every batch cycle.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) Monographs
    • US FDA 21 CFR Part 211 - cGMP for Finished Pharmaceuticals
    • Chinese Pharmacopoeia (ChP) guidelines for cardiovascular APIs

    Typical usage ratio

    • Stoichiometric to 1.5 mol equivalents relative to coupling agents, adjusted for impurity threshold as specified in specific monograph routes

    Downstream process integration

    • Enters the stepwise condensation and cyclization stage under controlled temperature (70–100°C) and anhydrous solvent conditions
    • Integrated in closed-system reactors with stringent in-process monitoring for residual solvents and by-products
    • Intermediates pass through preparative chromatography before final API crystallization and quality control assay

    Final product types

    • Tableted angiotensin receptor blockers (e.g., Losartan-type formulations)
    • Capsule-based antihypertensive drugs
    • Injectable solutions for acute hypertension management
    • Bulk API supplied for licensed formulation partners

    2. Advanced Agrochemical Synthesis—Herbicide Precursors

    Crop protection formulators utilize this intermediate in selective herbicide ingredient production, particularly where pyrimidine scaffolds deliver enhanced target binding. This compound forms part of the synthetic core for inhibitors targeting grass and broad-leaf weed enzymes. Manufacturers optimize batch yields by carefully controlling reactivity with chlorinated partners while adhering to global residue and registration standards. Finished actives are converted into water-dispersible granules and emulsifiable concentrates for field application.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH Regulation (1907/2006/EC) for environmental and toxicological safety
    • China National Standard GB 3796—Safety for Pesticide Products
    • OECD GLP Principles for agrochemical development

    Typical usage ratio

    • Normally 0.8–1.2 equivalents in reaction with acylating agents and subsequent sulfonamide coupling, adjusted per crop selectivity test data

    Downstream process integration

    • Introduced at the heterocycle formation stage of actives synthesis; monitored for formation of specific target isomers
    • Dosed under nitrogen atmosphere in batch reactors to limit hydrolytic breakdown
    • Intermediate purified via liquid-liquid extraction and crystallization prior to formulation blending

    Final product types

    • Water-dispersible granule herbicides for cereals and rice
    • Emulsifiable concentrate herbicide products for post-emergence control
    • Bulk active ingredient for agrochemical toll manufacturing
    • Pre-mixed tank formulation partners in integrated weed management

    3. Veterinary Drug Precursor for Livestock Feed Additives

    Animal health API producers integrate this material into the early-stage synthesis of pyrimidine-based agents for parasitic infection control in livestock. It serves as a key intermediate where strict residue control and purity levels are mandated. Chemical engineers batch-react the ingredient in enclosed vessels, following quality-by-design protocols for regulatory traceability. Formulators later convert APIs into medicated feed premixes and oral solutions conforming to veterinary approval pathways.

    Industry compliance standards

    • VICH GL3 Good Manufacturing Practice for APIs (Veterinary)
    • European Feed Additives Regulation (EC) No. 1831/2003
    • US FDA Guidance for Industry #218—Veterinary Drug Residue Control
    • GlobalGAP Livestock and Aquaculture Feed Standards

    Typical usage ratio

    • Dosed at equimolar levels with respect to subsequent chloroalkylating steps; range 1.0–1.3 mol equivalents depending on pathway efficiency

    Downstream process integration

    • Fed into the N-alkylation step post-initial pyrimidine ring assembly under low-light, low-oxygen conditions
    • Purity and residual impurity monitoring conducted using HPLC and mass spectrometry at this stage
    • Crude intermediate later processed into technical-grade API or micronized product

    Final product types

    • Oral solution antihelmintic drugs for cattle and swine
    • Medicated feed additive premixes in pellet or crumble forms
    • Veterinary API blends for further formulation
    • Quality-assured technical concentrate for regional licensees

    4. Specialty Fine Chemical Building Block for Custom Synthesis

    Fine chemical and custom synthesis providers purchase this molecule as a high-purity building block for small-molecule R&D programs and targeted library generation. Its stable structure and unique substitution pattern support SAR studies in pharmaceutical discovery or agrochemical pipeline validation. Synthesis teams apply this starting material under controlled microwave-assisted and flow-chemistry protocols with detailed analytical tracking for project-specific requirements.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System certification for specialty chemicals
    • GLP Standards for chemical R&D environments
    • US EPA TSCA Inventory communication, where relevant for export

    Typical usage ratio

    • Used in 1.0–2.0 equivalents, adjusted per reaction scale, stoichiometry, and required diversification in high-throughput synthesis

    Downstream process integration

    • Dissolved and charged as the first actionable substrate in diversified condensation or alkylation sequences
    • Reactors feature automated sampling points for NMR and liquid chromatography
    • Post-reaction intermediates isolated via high-vacuum distillation or preparative HPLC for parallel library creation

    Final product types

    • Custom reference compounds for pharmaceutical screening
    • Diversified small-molecule libraries for SAR optimization
    • Novel agrochemical candidates with proprietary structural features
    • Research-grade intermediates for patent-stage process development
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    Certification & Compliance
    More Introduction

    4-(4-Fluorophenyl)-6-Isopropyl-2-[(N-Methyl-N-Methylsulfonyl)Amino]Pyrimidinyl-5-Yl-Formyl: From Lab to Production Bench

    Unlocking Reliability Through Chemistry

    At our production site, 4-(4-Fluorophenyl)-6-Isopropyl-2-[(N-Methyl-N-Methylsulfonyl)Amino]Pyrimidinyl-5-Yl-Formyl doesn’t just start as a string of raw materials. Years of practice, adjustment, and operator experience go into shaping a process that yields this compound with the quality pharmaceutical and agrochemical innovators expect. While its IUPAC name isn’t the easiest to pronounce, those working in synthesis quickly recognize this molecule for its core: a pyrimidine ring that tolerates various process temperatures and provides downstream flexibility many pyrimidine analogs lack.

    Why the Structure Matters

    Designing, scaling, and reproducing a multi-step pyrimidine derivative calls for a different mindset than with more straightforward compounds. We deal daily with questions from project managers who want to know what makes this molecule stand out compared to common alternatives. Everything begins at the ring: incorporating a 4-fluorophenyl moiety at the 4-position brings benefits in terms of electronic distribution, which in turn influences solubility, reactivity, and binding behavior in target receptor applications. That fluorine is not just decorative — during scale-up, high purity fluorinated intermediates present specific challenges that our teams have already worked through with in-house analytics and in-situ monitoring.

    The isopropyl group at the 6-position is not an accident either. Over the years, we’ve seen how a bulky substituent here tends to restrict certain side reactions that disrupt yields. Legacy products with smaller substituents at this site have trouble matching the reproducibility under plant conditions — the results manifest as higher yields and cleaner downstream purifications.

    In the 2-position, N-methyl-N-methylsulfonyl functionality opens doors in terms of compatibility with further derivatizations. This feature makes our product a favorite among process chemists hunting for scaffolds to build new kinase inhibitors, antiviral leads, or crop protection candidates.

    Production-Centric Manufacturing

    Scaling up the manufacture of this compound doesn’t resemble textbook chemistry. We take pride in developing routes that tighten input control, maximize solvent recovery, and minimize batch deviations. The formyl group on the 5-position introduces sensitivity; not everyone can handle the safeguarding post-condensation, particularly when bulk orders start rolling in.

    We run reactors with carefully profiled temperature ramps and closely follow intermediate color and clarity. Every handling step, from material charging to vacuum swaps, reflects input from operators and floor managers who’ve solved real-world issues. Our engineers work beside R&D, so process glitches get addressed quickly. There’s significant benefit in not having to wait for a solution from a distant subcontractor.

    Model and Specifications from the Source

    We’ve tuned main output to a default specification range that suits regulatory and research expectations from API manufacturers, contract research organizations, and developers looking for clean pyrimidine cores. Every batch runs through our analytical suite, including NMR, HPLC, and LC-MS, which catch sub-percentage contaminants and provide a fingerprint that customers use for their own internal tracking. Today, the typical lot runs at high assay, and we’ve responded to requests for lots with tailored particle sizes or moisture levels.

    Our model synthesis grows out of continuous operator feedback. Earlier versions of the process exhibited slight color changes between lots. Solving for these led us to increase the distillation time of an early intermediate. Plant teams saw the impact: less “carryover” odor, greater consistency during crystallization, and reduced filter clogging. Such instantiation of process improvements shows why manufacturing the molecule ourselves, instead of relying on outside tollers or sub-suppliers, delivers tighter control year after year.

    Practical Usage Across Industries

    Synthetic organic chemists have sought out this compound for its scaffold versatility. Introductions of the N-methyl-N-methylsulfonyl fragment mean there’s plenty of room for custom modifications, opening the way for bioactive libraries and screenings. Researchers developing pharmaceutical intermediates prefer a material that already shows strong performance data for next-step derivatizations, saving both time and purification labor.

    Not every market sector applies this molecule the same way. In the pharma field, it can act as a clean building block for kinase inhibitor panels and small-molecule discovery programs. That same core, in agrochemicals, allows for design of actives that benefit from the electronic effects of fluorine and the spatial hindrance from isopropyl. Those working at bench or pilot scale see dramatic time savings when compared to multi-step preparations that start from scratch. This is not theory — several customers come back year-over-year for lots designed for custom projects, confident that bulk and repeat orders won’t just match last year’s material, they’ll show the same reactivity, the same impurity profile, lot after lot.

    Real-World Differences from Other Products

    Material hubs and distributors frequently ask what actually makes our batches different from unnamed equivalents on the market. As a manufacturer, we see real differences appear only after close work with end users. Some products on the market stem from a single route, never adjusted for scale. We’ve witnessed how subtle differences in input material source, solvent grade, or even drying temperature skew the formyl group’s reactivity or create persistent colored byproducts. Unlike traders, who may not even see the inside of a reactor, our process stays rooted in direct production. That’s where the “small changes” add up. For instance, a half-degree variance at the final recrystallization step might push material outside customer specifications for color or particle size. Receiving a call from a customer’s analytical chemist who’s struggling with slow dissolution in a screening run tells us we must review process logs, not just check a preset list of COA items.

    Products sourced from resellers can also carry more broad variability than what leaves our site. Materials sitting too long in uncontrolled environments pick up more than just moisture – they drift in purity, even before hitting project timelines for scalable syntheses. We store and ship our output under tightly defined conditions, short-listing warehouse or transit delays. Feedback loops with regular buyers highlight the value of reliable material: a project leader can plan pilot-scale runs confidently, knowing that last year’s compound, this month’s delivery, and next quarter’s option contracts rest on matched quality, not “averages.”

    Operator Knowledge Brings Repeatable Results

    The reality on site means often dealing with the unexpected — a valve that leaks, a bulk drum whose labeling is off, a pump that drops pressure mid-reaction. Practical knowledge and line experience overrule what paperwork can anticipate. We keep logs not out of compliance duty, but from a drive for outcomes: understanding when a shift in color means everything is on track, or when a baseline drift flags a deeper variable. Years ago, correcting a miscalibrated thermostat became the difference between spot-on formylation and an out-of-spec batch. That kind of experience won’t show up on a typical procurement spreadsheet, but it paves the way for batches that “just work” in follow-on chemistry.

    We’ve built trust over time with repeat buyers — whether a pharmaceutical developer or agrochemical pilot plant — who want to use their time generating value downstream, not troubleshooting supply inconsistencies. Returning customers often share feedback about reduced background noise in analytical traces, fewer purification cycles, and predictable crystal habits. These details seem minor, but for operators aiming for long campaign runs where a stop means not just lost time but wasted materials and downstream products, reliability matters most.

    Supporting Innovation and Ensuring Supply

    Downstream innovation depends fundamentally on predictable input. Every material leaving our plant reflects continuous engagement with payload developers who look to optimize every next stage. Often, these partners ask about yield percentages, impurity drift, or feasible scale-ups. We answer with documented runs, a willingness to run pilot lots, and a team ready to adapt conditions if research reveals new application challenges. We don’t operate in isolation: a field report from a contract manufacturer, or a bench note from an early-stage development chemist, feeds back to our own batch records and synthesis routines.

    Investments in new analytical instruments and increased staff training underline our commitment. We view material consistency as a function of both instrumentation and operator insight. Cross-training shop-floor workers means a greater likelihood of catching “off-notes” during early reaction stages, stopping issues before they move downstream. Regular site tours for customers demonstrate not just equipment, but commitment to up-close and hands-on manufacture. We share process data — not just “passes” and “fails” — without hiding problems behind fluffy language or abstract guarantees.

    Environmental and Compliance Transparency

    Production of halogenated pyrimidines brings with it clear compliance requirements. Safeguarding operator health, minimizing community impact, and aligning with evolving regulatory frameworks forms our operational baseline. Modernized ventilation, scrubbing, and waste-handling systems keep site exposures far below threshold limits. Continuous reviews with both local environmental oversight and independent auditors verify that emissions stay controlled, and we routinely adopt changes in solvent recovery or material substitution when new, greener options prove viable.

    We believe compliance shouldn’t rely on “check box” thinking. Real improvements – whether tighter trap monitoring for volatile organics or improved PPE routines for isopropyl intermediates – pay off not just for community and regulatory relationships, but in batch quality itself. We view sustainable operation and quality output as two sides of the same coin.

    Collaborating With the Community and Industry

    Direct manufacture offers a unique vantage point. We engage with university consortia, local trade associations, and standards promoters to share lessons learned — not every manufacturer is eager to discuss their actual routes or troubleshooting memories. Years of on-the-ground work, both on the plant floor and with lab colleagues, translate into a feedback network that shapes future chemistry. Conversations with downstream users of 4-(4-Fluorophenyl)-6-Isopropyl-2-[(N-Methyl-N-Methylsulfonyl)Amino]Pyrimidinyl-5-Yl-Formyl help steer investments in improved materials handling, faster batch releases, and expanded analytical capacity.

    Demand from biopharma and crop science sectors continues to grow, and we work with both established firms and ambitious startups bringing new ideas. For example, last year we welcomed a biotech partner looking to try unconventional kinase scaffolding, requiring us to spin up a special lot under new isolation conditions. That work not only expanded the partner’s options but gave our own team active insight into process tweaks for future lots.

    Looking Forward By Building on Core Strengths

    Each batch of 4-(4-Fluorophenyl)-6-Isopropyl-2-[(N-Methyl-N-Methylsulfonyl)Amino]Pyrimidinyl-5-Yl-Formyl represents hundreds of small adjustments, fixes, and operator insights. Manufacturing, at its heart, draws on both technical knowledge and practical lessons — you learn what makes certain crystallizations stall, which batches run fastest, and how to prevent the annoyances that throw off a carefully planned day.

    We aim to deepen our expertise not by chasing the latest buzzwords, but by continuing to listen to those working at every stage of research and manufacturing. That’s how supply chains become reliable, and chemistries become building blocks for new generations of discovery. The people who keep the reactors running, the analysts tweaking detection protocols, and the engineers building the next round of improvements work every day on the same problem: finding the shortest, most consistent path from feedstock to valuable end molecule. Each shipment is not just our product — it’s a reflection of a commitment to grounded expertise and the knowledge gained by working close to the chemistry itself.