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2-Methoxypyrimidin-5-amine

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Company Name: HaBo Hong Kong Co., Limited.
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Products Intro: Product Name:5-Amino-2-methoxypyrimidine
CAS:56621-89-7
Purity:0.98 Package:based on the requirments Remarks:Z
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Products Intro: Product Name:5-Amino-2-methoxypyrimidine
CAS:56621-89-7
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-04406
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Products Intro: Product Name:2-methoxypyrimidin-5-amine
CAS:56621-89-7
Purity:0.99 Package:25g
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Products Intro: Product Name:2-Methoxypyrimidin-5-amine
CAS:56621-89-7
Purity:99.0% Package:1KG;1USD
Company Name: Guangzhou Yuheng Pharmaceutical Technology Co., Ltd
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Products Intro: Product Name:2-methoxypyrimidin-5-amine
CAS:56621-89-7
Purity:0.97 Package:1KG;25KG

2-Methoxypyrimidin-5-amine manufacturers

2-Methoxypyrimidin-5-amine Basic information
Product Name:2-Methoxypyrimidin-5-amine
Synonyms:2-METHOXYPYRIMIDIN-5-AMINE;5-Pyrimidinamine, 2-methoxy;2-Methoxy-pyrimidin-5-ylamine;5-Pyrimidinamine, 2-methoxy- (9CI);5-Amino-2-methoxypyrimidine;2-Methoxypyrimidin-5-amine, 5-Amino-2-methoxy-1,3-diazine;2-Methoxy-5-pyriMidinaMine;2-methoxypyrimidine-5-amine
CAS:56621-89-7
MF:C5H7N3O
MW:125.13
EINECS:
Product Categories:Amines;Pyrazines, Pyrimidines & Pyridazines;PYRIMIDINE;Heterocycle-Pyrimidine series
Mol File:56621-89-7.mol
2-Methoxypyrimidin-5-amine Structure
2-Methoxypyrimidin-5-amine Chemical Properties
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
pka2.49±0.22(Predicted)
AppearanceYellow to brown Solid
InChIInChI=1S/C5H7N3O/c1-9-5-7-2-4(6)3-8-5/h2-3H,6H2,1H3
InChIKeyHKHRENFWPKWVML-UHFFFAOYSA-N
SMILESC1(OC)=NC=C(N)C=N1
Safety Information
Risk Statements 36/37/38
Safety Statements 26-36/37/39
HS Code 29335990
MSDS Information
2-Methoxypyrimidin-5-amine Usage And Synthesis
Synthesis
2-methoxy-5-nitropyrimidine

14001-69-5

2-Methoxypyrimidin-5-amine

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 materials2-methoxy-5-nitropyrimidine-->Hydrogen-->Methanol
Tag:2-Methoxypyrimidin-5-amine(56621-89-7) Related Product Information
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