ChemicalBook--->CAS DataBase List--->1239880-00-2

1239880-00-2

1239880-00-2 Structure

1239880-00-2 Structure
IdentificationBack Directory
[Name]

6-bromoimidazo[1,5-a]pyridine
[CAS]

1239880-00-2
[Synonyms]

6-bromoimidazo[1,5-a]pyridine
Imidazo[1,5-a]pyridine, 6-bromo-
[Molecular Formula]

C7H5BrN2
[MDL Number]

MFCD17677174
[MOL File]

1239880-00-2.mol
[Molecular Weight]

197.03
Chemical PropertiesBack Directory
[Melting point ]

240-246°C
[density ]

1.69±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

solid
[pka]

6.42±0.30(Predicted)
[color ]

Brown
[InChI]

1S/C7H5BrN2/c8-6-1-2-7-3-9-5-10(7)4-6/h1-5H
[InChIKey]

YLWZYCSSUYSOAW-UHFFFAOYSA-N
[SMILES]

Brc1ccc2cncn2c1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P264-P270-P301+P312-P302+P352-P305+P351+P338
[Hazard Codes ]

Xn
[Risk Statements ]

22-36/37/38
[Safety Statements ]

26
[WGK Germany ]

3
[HS Code ]

2933998090
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Hazard InformationBack Directory
[Uses]

6-Bromoimidazo[1,5-a]pyridine is a useful research chemical. It’s used in the preparation of substituted pyridazines as small mol. splicing modulator compds. for modulating splicing of mRNA.
[Synthesis]

Formamide, N-[(5-bromo-2-pyridinyl)methyl]-

1239880-13-7

6-bromoimidazo[1,5-a]pyridine

1239880-00-2

To a solution of N-((5-bromopyridin-2-yl)methyl)formamide (1.0 g, 4.6 mmol) in toluene (30 mL) was added phosphorus oxychloride (POCl3, 1.0 mL, 10.9 mmol). The reaction mixture was stirred at 103 °C for 2 h. After completion of the reaction, the mixture was concentrated to dryness under reduced pressure. The residue was dissolved in dichloromethane (DCM), washed sequentially with saturated aqueous sodium bicarbonate (NaHCO3) and brine, and the organic phase was dried with anhydrous sodium sulfate (Na2SO4), filtered and concentrated under reduced pressure. The residue was purified by fast column chromatography to afford the target product 6-bromoimidazo[1,5-A]pyridine (0.5 g, 55% yield) as a yellow solid. m/z 197,199 ([M+H]+) was detected by LC-MS.

[References]

[1] Patent: WO2016/112088, 2016, A1. Location in patent: Paragraph 0663
[2] Patent: US2010/204214, 2010, A1. Location in patent: Page/Page column 114
Spectrum DetailBack Directory
[Spectrum Detail]

6-bromoimidazo[1,5-a]pyridine(1239880-00-2)1HNMR
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