ChemicalBook > Product Catalog >Pharmaceutical intermediates >Heterocyclic compound >Pyridine compound >Chloropyridine >3-BROMO-5-CHLORO-2-METHOXY-PYRIDINE

3-BROMO-5-CHLORO-2-METHOXY-PYRIDINE

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Products Intro: Product Name:3-BROMO-5-CHLORO-2-METHOXY-PYRIDINE
CAS:102830-75-1
Purity:98% Package:1KG;5USD|1000KG;0.1USD
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Products Intro: Product Name:3-bromo-5-chloro-2-methoxypyridine
CAS:102830-75-1
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CAS:102830-75-1
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Products Intro: Product Name:3-BROMO-5-CHLORO-2-METHOXY-PYRIDINE
CAS:102830-75-1
Purity:98% Package:1kg;1USD
Company Name: Jinan Carbotang Biotech Co.,Ltd.
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Products Intro: Product Name:3-BROMO-5-CHLORO-2-METHOXY-PYRIDINE
CAS:102830-75-1
Purity:98% Package:5KG;1KG

3-BROMO-5-CHLORO-2-METHOXY-PYRIDINE manufacturers

3-BROMO-5-CHLORO-2-METHOXY-PYRIDINE Basic information
Product Name:3-BROMO-5-CHLORO-2-METHOXY-PYRIDINE
Synonyms:3-BROMO-5-CHLORO-2-METHOXY-PYRIDINE;2-Methoxy-3-Bromo-5-Chloropyridine;Pyridine,3-bromo-5-chloro-2-methoxy-;oro-2-methoxypyridine;3-BROMO-5-CHLORO-2-METHOXY-PYRIDINE ISO 9001:2015 REACH;2-methoxy-3-bromo-5-clopyridine
CAS:102830-75-1
MF:C6H5BrClNO
MW:222.47
EINECS:
Product Categories:Pyridine Series;Boronic Acid;Pyridine;Indoles ,Indazoles
Mol File:102830-75-1.mol
3-BROMO-5-CHLORO-2-METHOXY-PYRIDINE Structure
3-BROMO-5-CHLORO-2-METHOXY-PYRIDINE Chemical Properties
Melting point 49.0 to 53.0 °C
Boiling point 215.8±35.0 °C(Predicted)
density 1.650±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,Room Temperature
solubility soluble in Chloroform
form powder to crystal
pka-1.24±0.20(Predicted)
color White to Almost white
CAS DataBase Reference102830-75-1
Safety Information
Hazard Codes T
Risk Statements 25
Safety Statements 45
RIDADR UN 2811 6.1 / PGIII
HazardClass IRRITANT
HS Code 2933399990
MSDS Information
3-BROMO-5-CHLORO-2-METHOXY-PYRIDINE Usage And Synthesis
Synthesis
5-Chloro-2-methoxypyridine

13473-01-3

3-BROMO-5-CHLORO-2-METHOXY-PYRIDINE

102830-75-1

General procedure for the synthesis of 2-methoxy-3-bromo-5-chloropyridine from 2-methoxy-5-chloropyridine: 1. Glacial acetic acid solution of bromine was prepared by slowly adding bromine (1.5 mL, 29.28 mmol) to glacial acetic acid (7 mL). 2. 5-chloro-2-methoxypyridine (2.1 g, 14.63 mmol) and sodium acetate (1.2 g, 14.63 mmol) were dissolved in glacial acetic acid (7 mL) to form a mixture. 3. The bromine solution prepared in step 1 was slowly added to the mixture in step 2. 4. The resulting reaction mixture was stirred at 80 °C for 6 hours. 5. Upon completion of the reaction, the mixture was allowed to cool to room temperature. 6. Add ether and water to the cooled reaction mixture and extract. 7. The organic layer was separated and washed sequentially with 1N aqueous sodium hydroxide solution and 4% aqueous sodium bisulfite solution. 8. The organic layer was dried with magnesium sulfate and then the solvent was removed under reduced pressure. 9. The residue was purified by fast chromatography (100% hexane as eluent) to afford 2-methoxy-3-bromo-5-chloropyridine (2.1 g, 64% yield) as a white solid. 1H-NMR (300MHz, CDCl3) δ: 3.99 (s, 3H), 7.81 (d, 1H), 8.05 (d, 1H).

References[1] Journal of Heterocyclic Chemistry, 1985, vol. 22, p. 1583 - 1592
[2] Journal of Medicinal Chemistry, 1986, vol. 29, # 9, p. 1590 - 1595
[3] Patent: WO2012/69202, 2012, A1. Location in patent: Page/Page column 53
[4] Patent: EP2463289, 2012, A1. Location in patent: Page/Page column 21
[5] Patent: US5512575, 1996, A
3-BROMO-5-CHLORO-2-METHOXY-PYRIDINE Preparation Products And Raw materials
Raw materials5-Chloro-2-methoxypyridine
Tag:3-BROMO-5-CHLORO-2-METHOXY-PYRIDINE(102830-75-1) Related Product Information
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