ChemicalBook--->CAS DataBase List--->861673-68-9

861673-68-9

861673-68-9 Structure

861673-68-9 Structure
IdentificationBack Directory
[Name]

2-(2-(tert-butyl)phenoxy)pyridin-
[CAS]

861673-68-9
[Synonyms]

2-(2-(tert-butyl)phenoxy)pyridin-
2-[2-(1,1-Dimethylethyl)phenoxy]-3-Pyridinamine
3-Pyridinamine, 2-[2-(1,1-dimethylethyl)phenoxy]-
[Molecular Formula]

C15H18N2O
[MDL Number]

MFCD11156638
[MOL File]

861673-68-9.mol
[Molecular Weight]

242.32
Chemical PropertiesBack Directory
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P280-P305+P351+P338
Hazard InformationBack Directory
[Synthesis]

2-(2-tert-butyl-phenoxy)-3-nitro-pyridine

861673-67-8

2-(2-(tert-butyl)phenoxy)pyridin-

861673-68-9

Synthesis of 1b 2-(2-(tert-butyl)phenoxy)pyridin-3-amine: 1a 2-(2-tert-butyl-phenoxy)-3-nitropyridine (7.2 g, 26.5 mmol) was dissolved in a solvent mixture of methanol and ethyl acetate (160 mL, 1:1 v/v). 10% palladium carbon catalyst (360 mg, 0.33 mmol) was added and the reaction mixture was stirred overnight under hydrogen atmosphere. Upon completion of the reaction, the reaction mixture was filtered through a Celite pad to remove the catalyst and the filtrate was subsequently concentrated to afford 7.2 g (100% yield) of the target product 1b as a white powder. Mass spectral analysis: [M + H]+ = 243.

[References]

[1] Patent: WO2005/70920, 2005, A1. Location in patent: Page/Page column 64-65
[2] Patent: US2006/173002, 2006, A1. Location in patent: Page/Page column 40
[3] Patent: US2006/293522, 2006, A1. Location in patent: Page/Page column 19
[4] Patent: US2007/4677, 2007, A1. Location in patent: Page/Page column 23-24
[5] Bioorganic and Medicinal Chemistry Letters, 2013, vol. 23, # 14, p. 4206 - 4209
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