ChemicalBook--->CAS DataBase List--->286947-03-3

286947-03-3

286947-03-3 Structure

286947-03-3 Structure
IdentificationBack Directory
[Name]

5-BROMO-2-CHLORO-3-METHOXYPYRIDINE
[CAS]

286947-03-3
[Synonyms]

5-BROMO-2-CHLORO-3-METHOXYPYRIDINE
2-CHLORO-3-METHOXY-5-BROMOPYRIDINE
Pyridine, 5-bromo-2-chloro-3-methoxy-
[Molecular Formula]

C6H5BrClNO
[MDL Number]

MFCD08234976
[MOL File]

286947-03-3.mol
[Molecular Weight]

222.47
Chemical PropertiesBack Directory
[Melting point ]

68-72°C
[Boiling point ]

245.6±35.0 °C(Predicted)
[density ]

1.650±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[form ]

solid
[pka]

-3.02±0.10(Predicted)
[color ]

White to off-white
[InChI]

InChI=1S/C6H5BrClNO/c1-10-5-2-4(7)3-9-6(5)8/h2-3H,1H3
[InChIKey]

GFJMOZYIDADKLJ-UHFFFAOYSA-N
[SMILES]

C1(Cl)=NC=C(Br)C=C1OC
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)Skull and Crossbones (GHS06)
GHS05,GHS06
[Signal word ]

Danger
[Hazard statements ]

H301-H318
[Precautionary statements ]

P280-P301+P310-P305+P351+P338
[Hazard Codes ]

Xn,T
[Risk Statements ]

22-41-25
[Safety Statements ]

26-39-45
[RIDADR ]

2811
[WGK Germany ]

3
[HazardClass ]

IRRITANT
[PackingGroup ]

[HS Code ]

2933399990
[Storage Class]

6.1D - Non-combustible acute toxic Cat.3
toxic hazardous materials or hazardous materials causing chronic effects
[Hazard Classifications]

Acute Tox. 3 Oral
Eye Dam. 1
Spectrum DetailBack Directory
[Spectrum Detail]

5-BROMO-2-CHLORO-3-METHOXYPYRIDINE(286947-03-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

5-BROMO-2-CHLORO-PYRIDIN-3-OL

286946-77-8

Iodomethane

74-88-4

5-BROMO-2-CHLORO-3-METHOXYPYRIDINE

286947-03-3

Step 3: Synthesis of 5-bromo-2-chloro-3-methoxypyridine 5-Bromo-2-chloro-3-hydroxypyridine (1.88 g, 9 mmol), iodomethane (1.42 g, 10 mmol) and potassium carbonate (K2CO3, 2.76 g, 20 mmol) were dissolved in acetonitrile. The reaction mixture was stirred at 80 °C for 4 hours. After completion of the reaction, the solvent was removed by evaporation and the residue was dissolved in dichloromethane (CH2Cl2). The resulting solution was washed with water and the organic phase was dried over anhydrous sodium sulfate and concentrated. Finally, the target product 5-bromo-2-chloro-3-methoxypyridine (1.62 g, 81% yield) was purified by silica gel column chromatography. Mass spectrum (ESI) m/z: 223.9 [M + 1].

[References]

[1] Patent: EP2952510, 2015, A1. Location in patent: Paragraph 0148
[2] Patent: US2002/19388, 2002, A1
[3] Journal of Medicinal Chemistry, 2007, vol. 50, # 15, p. 3627 - 3644
[4] Patent: EP1147112, 2003, B1. Location in patent: Page/Page column 35
[5] Patent: US2003/225268, 2003, A1. Location in patent: Page 31-32
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