ChemicalBook--->CAS DataBase List--->1260863-86-2

1260863-86-2

1260863-86-2 Structure

1260863-86-2 Structure
IdentificationBack Directory
[Name]

6-Bromooxazolo[4,5-b]pyridine
[CAS]

1260863-86-2
[Synonyms]

6-Bromooxazolo[4,5-b]pyridine
Oxazolo[4,5-b]pyridine, 6-bromo-
[EINECS(EC#)]

200-258-5
[Molecular Formula]

C6H3BrN2O
[MDL Number]

MFCD13193309
[MOL File]

1260863-86-2.mol
[Molecular Weight]

199
Chemical PropertiesBack Directory
[Boiling point ]

244.0±20.0 °C(Predicted)
[density ]

1.826±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[pka]

-2.51±0.50(Predicted)
[Appearance]

Light yellow to brown Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P264-P280-P302+P352-P321-P332+P313-P362-P264-P270-P301+P312-P330-P501-P264-P280-P305+P351+P338-P337+P313P
Spectrum DetailBack Directory
[Spectrum Detail]

6-Bromooxazolo[4,5-b]pyridine(1260863-86-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-amino-5-bromopyridin-3-ol

39903-01-0

Triethyl orthoformate

122-51-0

6-Bromooxazolo[4,5-b]pyridine

1260863-86-2

General procedure for the synthesis of 6-bromooxazolo[4,5-b]pyridine from 3-hydroxy-2-amino-5-bromopyridine and triethyl orthoformate: 2-amino-5-bromo-3-hydroxypyridine (200 mg, 1.06 mmol) was dissolved in 3 mL of triethyl orthoformate and a catalytic amount of p-toluenesulfonic acid was added. The reaction mixture was heated to reflux for 5 hours. After completion of the reaction, it was cooled to room temperature, diluted with dichloromethane (DCM) and washed with saturated sodium bicarbonate solution. The organic phase was dried with anhydrous sodium sulfate and subsequently concentrated to dryness under reduced pressure. The residue was purified by fast column chromatography to give 212 mg (60% yield) of 6-bromoxazolo[4,5-b]pyridine.

[References]

[1] Patent: WO2011/15343, 2011, A1. Location in patent: Page/Page column 40
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