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4-Bromo-2-methoxypyridine

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CAS:100367-39-3
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  • 4-Bromo-2-methoxypyridine
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  • $200.00 / 1KG
  • 2025-09-25
  • CAS:100367-39-3
  • Min. Order: 1KG
  • Purity: 99%, 99.5% Sublimated
  • Supply Ability: g-kg-tons, free sample is available
4-Bromo-2-methoxypyridine Basic information
Product Name:4-Bromo-2-methoxypyridine
Synonyms:4-BROMO-2-METHOXYPYRIDINE;2-Methoxy-4-broMoquinoline;4-Bromo-2-Methoxypyridine(WX637041);Pyridine,4-bromo-2-methoxy-;4-Bromo-2-methoxypyridine ISO 9001:2015 REACH
CAS:100367-39-3
MF:C6H6BrNO
MW:188.02
EINECS:
Product Categories:Heterocycle-Pyridine series;alkyl bromide;Pyridine Series;blocks;Bromides;Pyridines;Pyridine
Mol File:100367-39-3.mol
4-Bromo-2-methoxypyridine Structure
4-Bromo-2-methoxypyridine Chemical Properties
Melting point 25-26℃
Boiling point 87℃/15mm
density 1.530±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka3.76±0.10(Predicted)
form Low Melting Solid
color Off-white to pale yellow
Water Solubility Slightly soluble in water.
InChIInChI=1S/C6H6BrNO/c1-9-6-4-5(7)2-3-8-6/h2-4H,1H3
InChIKeyYFTGMMXMLPTTAY-UHFFFAOYSA-N
SMILESC1(OC)=NC=CC(Br)=C1
Safety Information
Hazard Codes Xi
Safety Statements 24/25
HS Code 29339900
MSDS Information
4-Bromo-2-methoxypyridine Usage And Synthesis
Uses4-Bromo-2-methoxypyridine used in the synhesis of Imidazo [1, 2-a] pyrimidines. Suzuki coupling between 4-methoxyphenylboronic acid and 4-bromo-2-methoxypyridine affords 1, 5-disubstituted pyridones. Starting material used in a synthesis of crown-ester-bipyridines and viologens via sodium or nickel reductive coupling, side chain oxidation and esterification.
Synthesis
4-Bromo-2-fluoropyridine

128071-98-7

Sodium Methoxide

124-41-4

4-Bromo-2-methoxypyridine

100367-39-3

A non-homogeneous reaction mixture formed by 4-bromo-2-fluoropyridine (2.64 mL, 25.6 mmol) and sodium methanolate (8.29 g, 153 mmol) in methanol (36.5 mL) was placed in a pressure tube and reacted for 5 hours at 155°C. Upon completion of the reaction, the mixture was cooled to room temperature, filtered to remove the solid insoluble material and the solids were washed with ethyl acetate. The filtrate was concentrated to give a light yellow oil containing a small amount of white solid. The yellow oily material was decanted, diluted with water and the aqueous phase was extracted with ethyl acetate (2×). The organic layers were combined, washed sequentially with water and saturated saline, dried over anhydrous magnesium sulfate, filtered and concentrated to afford the target product 4-bromo-2-methoxypyridine (4.43 g, 21.20 mmol, 83% yield) as a yellow oil.LC-MS analysis: the calculated value of C6H6BrNO was 188.02, and the measured values of [M + H]+ were 187.9, 189.9. 1H NMR was used as the analyte. 189.9. 1H NMR (400 MHz, CDCl3) δ 7.98 (d, J = 5.5 Hz, 1H), 7.02 (dd, J = 5.5, 1.5 Hz, 1H), 6.94 (d, J = 1.8 Hz, 1H), 3.92 (s, 3H).

References[1] Patent: WO2015/171722, 2015, A1. Location in patent: Page/Page column 67
4-Bromo-2-methoxypyridine Preparation Products And Raw materials
Raw materials4-Bromo-2-fluoropyridine-->Sodium Methoxide
Preparation Products1-(2-Hydroxyethyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2(1H)-one
Tag:4-Bromo-2-methoxypyridine(100367-39-3) Related Product Information
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