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Postion:Product Catalog >Pharmaceutical intermediates>Heterocyclic compound>Pyrimidines>Methoxy-pyrimidine>2-Amino-4-methoxypyrimidine
2-Amino-4-methoxypyrimidine
  • 2-Amino-4-methoxypyrimidine
  • 2-Amino-4-methoxypyrimidine
  • 2-Amino-4-methoxypyrimidine

2-Amino-4-methoxypyrimidine NEW

Price Get Latest Price
Package 200kg
Min. Order: 200kg
Supply Ability: 20 tons
Update Time: 2025-04-08

Product Details

Product Name: 2-Amino-4-methoxypyrimidine CAS No.: 155-90-8
Min. Order: 200kg Purity: ≥99%
Supply Ability: 20 tons Release date: 2025/04/08

2-Amino-4-methoxypyrimidine (CAS No.: 155-90-8) – Technological Innovations and Market Opportunities for Pyrimidine Drug Intermediates

I. Basic Information and Physicochemical Properties

Chinese Name: 2-Amino-4-methoxypyrimidine
English Name: 2-Amino-4-methoxypyrimidine
CAS No.: 155-90-8
Molecular Formula: C?H?N?O
Molecular Weight: 125.13
Appearance: White to light yellow crystalline powder
Melting Point: 150-152℃
Boiling Point: 328℃ (atmospheric pressure)
Density: 1.26 g/cm3
Solubility: Slightly soluble in water (0.5g/100mL, 25℃), easily soluble in methanol, ethanol, DMF, and other polar solvents.

Chemical Properties:

  • Basicity: The amino group (-NH?) confers weak basicity (pKa≈9.8), allowing salt formation with acids.

  • Reactivity: The methoxy group (-OCH?) at the 4-position undergoes nucleophilic substitution reactions, reacting with reagents such as halogenated hydrocarbons and amines to form derivatives.

  • Stability: Stable to acids, but prone to hydrolysis and demethoxylation under strong alkaline conditions.

II. Upstream and Downstream Industry Chain Analysis

Upstream Raw Materials and Synthesis Process

Core Raw Materials:

  • 4-Methoxypyrimidine-2-one (CAS: 5245-59-2)

  • Ammonia water (NH?·H?O)

Synthesis Route:

  1. Step 1: 4-Methoxypyrimidine-2-one reacts with excess ammonia water in a high-pressure reactor at 150-180℃ and 3-5 MPa for 12-16 hours.

  2. Step 2: After cooling and crystallization, the product is filtered and recrystallized from ethanol to obtain a purity ≥99% with a yield of 78-82%.

Downstream Products and Derivatives

Pharmaceutical Field:

  • Antimalarial Drugs: Reacts with haloalkanes to form 2-alkylamino-4-methoxypyrimidine, a precursor for synthesizing mefloquine.

  • Anticancer Drugs: Serves as an intermediate for tyrosine kinase inhibitors, used in synthesizing EGFR-targeted drugs (e.g., a key intermediate for osimertinib).

Agrochemical Field:

  • Herbicides: Condenses with triazine compounds to form pyrimidine-oxybenzoic acid herbicides (e.g., pyriminoether), effective against annual grass weeds.

  • Fungicides: Synthesized via oximination reactions to produce pyrimidine oxime fungicides, showing significant efficacy against wheat rust.

Materials Science:

  • Organic Semiconductors: Copolymerizes with thiophene to prepare conjugated polymers for organic field-effect transistors (OFETs).

  • Fluorescent Materials: Modified with fluorescent groups to prepare biological probes for live-cell imaging.

III. Analysis of Core Application Areas

  1. Pharmaceutical R&D

    • Antimalarial Drug Innovation:
      2-Amino-4-methoxypyrimidine condenses with 1,3-dichloroacetone to form a key intermediate for mefloquine, which has 5 times the antimalarial activity of traditional drug quinine and low drug resistance.

    • Antiviral Drugs:
      Acts as a nucleoside analog precursor for synthesizing anti-influenza drugs (e.g., favipiravir intermediates), inhibiting RNA polymerase activity.

  2. Agrochemical Creation

    • Selective Herbicides:
      Reacts with 2,4-dichlorophenoxyacetic acid ethyl ester to form pyrimidine-oxyphenoxypropionic acid herbicides, achieving over 95% control efficacy against barnyard grass in rice fields.

    • Novel Fungicides:
      Introduces methoxy groups to synthesize pyrimidine methoxyacrylate fungicides, providing 91% control efficacy against cucumber powdery mildew with a duration of over 15 days.

  3. Advanced Materials

    • Organic Optoelectronic Materials:
      Copolymerizes with fluorene compounds to prepare blue-emitting materials, with OLED devices achieving an external quantum efficiency (EQE) of 25% and a lifetime exceeding 10,000 hours.

    • Lithium-ion Batteries:
      Used as an electrolyte additive to form a stable SEI film on the electrode surface, enhancing battery cycle life to over 2000 cycles.

IV. Technological Advantages and Market Dynamics

Technological Barriers:

  • The amination reaction requires high-pressure conditions. Adopting continuous flow microreaction technology shortens the reaction time to 6 hours and reduces energy consumption by 40%.

Capacity Distribution:

  • Global annual production capacity is approximately 200 tons, with China accounting for 65%. Major manufacturers include Zhejiang Hisoar Pharmaceutical and Jiangsu Lianhua Technology.

Market Demand:

  • Driven by demand for antimalarial drugs and novel agrochemicals, the demand for this intermediate increased by 22% year-on-year in 2024, and the market size is expected to exceed 50 million yuan in 2025.

V. Safety and Storage Recommendations

Hazards:

  • Mildly irritating to the skin. Wear protective gloves and goggles during handling.

Storage Conditions:

  • Store in a sealed container in a cool, dry place (≤25℃), protected from light and moisture, and away from strong acids and bases.


This translation maintains the original format and technical details while ensuring accuracy and professionalism.


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