2-Methoxypyrimidin-5-amine
- Product Name
- 2-Methoxypyrimidin-5-amine
- CAS No.
- 56621-89-7
- Chemical Name
- 2-Methoxypyrimidin-5-amine
- Synonyms
- 2-Methoxy-5-pyriMidinaMine;2-METHOXYPYRIMIDIN-5-AMINE;5-Pyrimidinamine, 2-methoxy;5-Amino-2-methoxypyrimidine;2-methoxypyrimidine-5-amine;2-Methoxy-pyrimidin-5-ylamine;5-Pyrimidinamine, 2-methoxy- (9CI);2-Methoxypyrimidin-5-amine ISO 9001:2015 REACH;2-Methoxypyrimidin-5-amine, 5-Amino-2-methoxy-1,3-diazine
- CBNumber
- CB9332124
- Molecular Formula
- C5H7N3O
- Formula Weight
- 125.13
- MOL File
- 56621-89-7.mol
2-Methoxypyrimidin-5-amine Property
- Melting point:
- 119-120 °C(Solv: benzene (71-43-2))
- Boiling point:
- 294.4±32.0 °C(Predicted)
- Density
- 1.224±0.06 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2–8 °C
- pka
- 2.49±0.22(Predicted)
- Appearance
- Yellow to brown Solid
- InChI
- InChI=1S/C5H7N3O/c1-9-5-7-2-4(6)3-8-5/h2-3H,6H2,1H3
- InChIKey
- HKHRENFWPKWVML-UHFFFAOYSA-N
- SMILES
- C1(OC)=NC=C(N)C=N1
Safety
- Risk Statements
- 36/37/38
- Safety Statements
- 26-36/37/39
- HS Code
- 29335990
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- M332998
- Product name
- 2-Methoxypyrimidin-5-amine
- Packaging
- 100mg
- Price
- $60
- Updated
- 2021/12/16
- Product number
- M332998
- Product name
- 2-Methoxypyrimidin-5-amine
- Packaging
- 500mg
- Price
- $155
- Updated
- 2021/12/16
- Product number
- 4H30-1-X9
- Product name
- 5-Amino-2-methoxypyrimidine
- Purity
- 95%
- Packaging
- 5G
- Price
- $316
- Updated
- 2021/12/16
- Product number
- 4H30-1-X9
- Product name
- 5-Amino-2-methoxypyrimidine
- Purity
- 95%
- Packaging
- 1g
- Price
- $79
- Updated
- 2021/12/16
- Product number
- W7025
- Product name
- 5-Amino-2-methoxypyrimidine
- Packaging
- 250mg
- Price
- $87
- Updated
- 2021/12/16
2-Methoxypyrimidin-5-amine Chemical Properties,Usage,Production
Synthesis
14001-69-5
56621-89-7
Example 40: Synthesis of 4-[2-(difluoromethyl)-4-methoxy-1H-benzimidazol-1-yl]-N-(2-methoxy-5-pyrimidinyl)-6-(4-morpholinyl)-1,3,5-triazin-2-amine The target compound was synthesized according to Method A. To a solution of sodium methanol (0.090 g sodium) in methanol (12 mL) was added 0.486 g (3.03 mmol) of 2-chloro-5-nitropyrimidine, and the mixture was heated under reflux conditions for 1 hour. After completion of the reaction, the mixture was cooled, concentrated in vacuum, extracted with ethyl acetate and washed with water. The aqueous layer was extracted with chloroform, the organic layers were combined, dried over anhydrous sodium sulfate and concentrated to give 0.347 g (75% yield) of 2-methoxy-5-nitropyrimidine as a yellow powder.1H NMR (CDCl3) δ 9.31 (s, 2H), 4.17 (s, 3H); LCMS (APCI+) m/z: 156 (MH+, 100%). 0.342 g (2.20 mmol) of the above nitro compound was dissolved in methanol (20 mL), 0.30 g of 10% Pd/C catalyst was added, and the reaction was stirred for 18 hr under a hydrogen atmosphere (25 in/hr). After completion of the reaction, the reaction mixture was filtered through diatomaceous earth and the filtrate was concentrated to give 0.274 g (100% yield) of 5-amino-2-methoxypyrimidine as a colorless oil.1H NMR (DMSO-d6) δ 8.05 (s, 2H), 3.94 (s, 3H); LCMS (APCI+) m/z: 126 (MH+, 100%). 0.274 g (2.19 mmol) of the above amino compound was dissolved in tetrahydrofuran (3 mL), 1.25 mL of NaHMDS (2M THF solution) was added and stirred for 10 min. Then 0.31 g (0.78 mmol) of 1-[4-chloro-6-(4-morpholinyl)-1,3,5-triazin-2-yl]-2-(difluoromethyl)-4-methoxy-1H-benzimidazole solution in THF (5 mL) was added and stirring was continued for 90 minutes. After completion of the reaction, the reaction mixture was neutralized with acetic acid, diluted with water and extracted with ethyl acetate. The organic layer was washed sequentially with water and ammonia, dried and concentrated. Recrystallization by ethanol/dichloromethane gave 0.098 g (26% yield) of the target compound with melting point 255-258 °C.1H NMR (DMSO-d6) δ 10.07 (s, 1H), 8.88-8.74 (m, 2H), 8.15-7.42 (m, 3H), 6.97 (d, J = 8.0 Hz, 1H), 3.98 (s, 3H), 3.93 (s, 3H), 3.82-3.72 (m, 8H); Elemental Analysis Calculated Values C21H21F2N6O3: C, 52.0; H, 4.4; N, 26.0. Measured Values: C, 52.1; H, 4.5; N, 26.0%.
References
[1] Patent: US2011/9405, 2011, A1. Location in patent: Page/Page column 55-56
2-Methoxypyrimidin-5-amine Preparation Products And Raw materials
Raw materials
Preparation Products
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View Lastest Price from 2-Methoxypyrimidin-5-amine manufacturers
- Product
- 2-Methoxypyrimidin-5-amine 56621-89-7
- Price
- US $1.10/g
- Min. Order
- 1g
- Purity
- 99.00%
- Supply Ability
- 100 Tons Min
- Release date
- 2021-12-10
- Product
- 2-Methoxypyrimidin-5-amine 56621-89-7
- Price
- US $1.00/KG
- Min. Order
- 1KG
- Purity
- 99.0%
- Supply Ability
- 100kg
- Release date
- 2020-01-07