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Postion:Product Catalog >Pharmaceutical intermediates>Heterocyclic compound>Pyrimidines>Methoxy-pyrimidine>4-Pyrimidinamine, 5-methoxy- (9CI)
4-Pyrimidinamine, 5-methoxy- (9CI)
  • 4-Pyrimidinamine, 5-methoxy- (9CI)
  • 4-Pyrimidinamine, 5-methoxy- (9CI)
  • 4-Pyrimidinamine, 5-methoxy- (9CI)

4-Pyrimidinamine, 5-methoxy- (9CI) NEW

Price Get Latest Price
Package 200kg
Min. Order: 200kg
Supply Ability: 20 tons
Update Time: 2025-04-09

Product Details

Product Name: 4-Pyrimidinamine, 5-methoxy- (9CI) CAS No.: 695-86-3
Min. Order: 200kg Purity: ≥99%
Supply Ability: 20 tons Release date: 2025/04/09

4-Amino-5-methoxypyrimidine (CAS No.: 695-86-3) – Technical and Market Analysis of High-Value Pyrimidine Intermediates

I. Basic Information and Physicochemical Properties

  1. Key Chemical Parameters

    • Chinese Name: 4-Amino-5-methoxypyrimidine

    • English Name: 4-Amino-5-methoxypyrimidine

    • CAS No.: 695-86-3

    • Molecular Formula

    • Molecular Weight: 125.13

    • Appearance: White to off-white crystalline powder, odorless, low hygroscopicity.

  2. Physicochemical Properties

    • Alkalinity: Weakly basic at the 4-amino group (pKa≈5.2); forms salts with inorganic acids (e.g., hydrochloride, sulfate).

    • Reactivity:

    • Stability: Stable at room temperature; decomposes under strong oxidants or high temperatures (>200℃). Store in a dark, dry place.

    • 5-methoxy group is stable; 4-amino group undergoes acylation, alkylation.

    • Ring nitrogen atoms participate in coordination and nucleophilic substitution.

    • Soluble in methanol, ethanol, DMF, etc.

    • Slightly soluble in water (≈1.5g/100mL at 25℃).

    • Insoluble in ether.

    • Melting Point: 168-170℃

    • Boiling Point: 365℃ (atmospheric pressure)

    • Density: 1.29 g/cm³

    • Solubility:

    • Chemical Characteristics:

II. Upstream-Downstream Industry Chain Analysis

  1. Upstream Raw Materials and Synthesis Process

    • High-Pressure Ammonolysis Method:
      5-Methoxypyrimidine-4-one reacts with excess ammonia solution in the presence of a copper-based catalyst (e.g., CuO/Al₂O₃) at 170-190℃ and 6-8MPa for 10-14 hours.
      Purified product (≥99% purity) is obtained via acidification, neutralization, and recrystallization, with a yield of 75-80%.
      Reaction Equation:

    • 5-Methoxypyrimidine-4-one (CAS: 23297-69-0)

    • Ammonia solution (NH₃・H₂O) or liquid ammonia.

    • Core Raw Materials:

    • Mainstream Synthesis Route:

  2. Downstream Products and Derivatives

    • Metal-Organic Catalysts: Pd-pyrimidine complexes for Suzuki-Miyaura coupling reactions.

    • Optoelectronic Materials: Hole-transport layer component in OLED devices (EQE up to 22%).

    • Herbicides: Key intermediate for pyrazosulfuron-ethyl (selective control of weeds in rice fields).

    • Fungicides: Precursor for pyrimidinylmethoxyacrylate fungicides (90%+ efficacy against powdery mildew).

    • Antimalarial Drugs: Intermediate for Malaridine (inhibits Plasmodium DNA polymerase).

    • Antiviral Drugs: Precursor for HCV drugs (e.g., sofosbuvir intermediates).

    • Anticancer Drugs: Scaffold for thymidylate synthase inhibitors (e.g., 5-fluorouracil derivatives).

    • Pharmaceutical Intermediates:

    • Agrochemical Intermediates:

    • Materials and Fine Chemicals:

III. Key Application Fields

  1. Pharmaceutical R&D and Innovative Drugs

    • Antimalarial Intermediates: Condensation with haloarenes yields malaridine intermediates, effective against drug-resistant malaria.

    • Antiviral Precursors: Nucleoside analogs (e.g., HCV RNA polymerase inhibitors) with >95% clinical cure rates.

    • Anticancer Drug Synthesis: Fluorouracil derivatives disrupt tumor cell DNA synthesis (used in gastric/colorectal cancer).

  2. Agrochemical Innovation and Green Plant Protection

    • Herbicide Intermediates: Reaction with 2,4-D esters produces pyrazosulfuron-ethyl intermediates (10-15g/ha dosage).

    • Novel Fungicides: Pyrimidinylmethoxyacrylate derivatives with 14-day residual efficacy.

  3. Materials Science and Catalysis

    • Catalyst Ligands: Pd-pyrimidine complexes enhance catalytic efficiency by 30% in Suzuki-Miyaura reactions.

    • Organic Optoelectronics: Copolymerized with thiophenes for high-mobility OLED hole-transport layers.

IV. Technological Advantages and Market Dynamics

  • Technical Barriers:

    • High-pressure ammonolysis requires precise catalyst control. Microchannel flow technology reduces reaction time to 5 hours, lowers impurities to <0.1%, and increases yields to 85%.

  • Production Capacity:

    • Global capacity ≈100 tons/year; China accounts for 70% (major producers: Zhejiang Yongtai Technology, Jiangsu Zhongqi Technology).

  • Market Demand:

    • Driven by antimalarial, HCV, and agrochemical demand, 2024 demand grew 20% YoY. 2025 market projected to exceed $40 million, with pharmaceuticals dominating 70%.

V. Safety and Storage Recommendations

  • Hazards:

    • Dust irritates eyes/respiratory tract; LD50 >2000mg/kg (oral, rat). Wear dust masks/gloves.

  • Storage:

    • Seal in cool, dry conditions (≤25℃); use moisture-barrier packaging (e.g., foil bags). Avoid oxidizers/acids.

VI. SEO Optimization Strategy

  1. Keyword Layout

    • Core Keywords: 4-Amino-5-methoxypyrimidine, 695-86-3, pyrimidine intermediates, antimalarial API, pyrazosulfuron intermediate.

    • Long-Tail Keywords: 4-Amino-5-methoxypyrimidine synthesis, HCV drug intermediates, metal-organic catalyst ligands.


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