
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:
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.
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
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.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.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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- Since: 2004-04-13
- Address: No. 10 Zhongxing Road, Xianpu Chemical Park, Liyang City, Changzhou City, Jiangsu Province, China