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220513-46-2

220513-46-2 Structure

220513-46-2 Structure
IdentificationBack Directory
[Name]

6-Bromo-8-fluoroquinoline
[CAS]

220513-46-2
[Synonyms]

6-Bromo-8-fluoroquinoline
6-Bromo-8-fluoroquinoline95%
Quinoline, 6-bromo-8-fluoro-
6-Bromo-8-fluoroquinoline 95%
6-Bromo-8-fluoro-1-azanaphthalene
Cyclobutanecarboxylicacid,8-oxo-,phenylmethylester
[EINECS(EC#)]

604-604-1
[Molecular Formula]

C9H5BrFN
[MDL Number]

MFCD11053791
[MOL File]

220513-46-2.mol
[Molecular Weight]

226.05
Chemical PropertiesBack Directory
[Melting point ]

104-106°C
[Boiling point ]

294.9±20.0 °C(Predicted)
[density ]

1.647±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,Room Temperature
[form ]

crystalline powder
[pka]

1.14±0.20(Predicted)
[color ]

Pale yellow
[InChI]

InChI=1S/C9H5BrFN/c10-7-4-6-2-1-3-12-9(6)8(11)5-7/h1-5H
[InChIKey]

DDCOYWOYIUEOHQ-UHFFFAOYSA-N
[SMILES]

N1C2C(=CC(Br)=CC=2F)C=CC=1
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22-37/38-41
[Safety Statements ]

26-39
[WGK Germany ]

3
[HazardClass ]

IRRITANT
[HS Code ]

2933499090
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Eye Dam. 1
Skin Irrit. 2
STOT SE 3
Spectrum DetailBack Directory
[Spectrum Detail]

6-Bromo-8-fluoroquinoline(220513-46-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

4-Bromo-2-fluoroaniline

367-24-8

Glycerol

56-81-5

6-Bromo-8-fluoroquinoline

220513-46-2

General procedure for the synthesis of 6-bromo-8-fluoroquinoline from 4-bromo-2-fluoroaniline and glycerol: 3-nitrobenzenesulfonic acid sodium salt (0.48 g, 2.132 mmol) and glycerol (0.516 ml, 7.06 mmol) were added to a concentrated H2SO4 (0.63 ml, 11.82 mmol) and H2O (0.48 ml, 26.6 mmol) solution to form a thick gray suspension. The mixture was heated to 110°C. 4-Bromo-2-fluoroaniline was added in batches over a period of 10 min, during which the temperature was raised to 95°C. The reaction mixture was then heated to 140 °C and stirred overnight. Upon completion of the reaction, the reaction mixture was cooled, poured into water and the pH was adjusted with ammonia to 7. The brown precipitate formed was collected by filtration and partially dried. The resulting solid (0.63 g) was purified by fast column chromatography to afford 6-bromo-8-fluoroquinoline (0.4 g, 1.77 mmol, 88% yield).

[References]

[1] Patent: WO2009/50204, 2009, A1. Location in patent: Page/Page column 15; 48-49
[2] Patent: WO2018/116072, 2018, A1. Location in patent: Page/Page column 97; 98
[3] Patent: CN105968115, 2016, A. Location in patent: Paragraph 0449-0451
[4] Patent: WO2010/20363, 2010, A1. Location in patent: Page/Page column 131-132
[5] Journal of Medicinal Chemistry, 2010, vol. 53, # 10, p. 4066 - 4084
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