ChemicalBook--->CAS DataBase List--->29449-82-9

29449-82-9

29449-82-9 Structure

29449-82-9 Structure
IdentificationBack Directory
[Name]

2-[(6-Chloro-2-pyridinyl)amino]-1-ethanol
[CAS]

29449-82-9
[Synonyms]

2-chloro-6-ethanolaminopyridine
2-((6-Chloropyridin-2-yl)amino)ethanol
2-[(6-Chloro-2-pyridinyl)amino]-1-ethanol
[Molecular Formula]

C7H9ClN2O
[MDL Number]

MFCD13562421
[MOL File]

29449-82-9.mol
[Molecular Weight]

172.61
Chemical PropertiesBack Directory
[Boiling point ]

356.0±27.0 °C(Predicted)
[density ]

1.347±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[pka]

14.50±0.10(Predicted)
Safety DataBack Directory
[HazardClass ]

IRRITANT
Hazard InformationBack Directory
[Synthesis]

2,6-Dichloropyridine

2402-78-0

Monoethanolamine

141-43-5

2-[(6-Chloro-2-pyridinyl)amino]-1-ethanol

29449-82-9

The general procedure for the synthesis of 2-((6-chloropyridin-2-yl)amino)ethanol from 2,6-dichloropyridine and 2-aminoethanol was as follows: referring to the method of Example 67, 2-aminoethanol (0.82 g, 13.5 mmol) was added to a pyridine solution (10 mL) containing 2,6-dichloropyridine (2.0 g, 13.5 mmol) and the reaction was at room temperature The reaction was carried out at room temperature. Subsequently, the reaction mixture was heated to 100 °C and kept overnight. After completion of the reaction, the mixture was concentrated under vacuum to give a residue. The residue was dissolved in ethyl acetate, washed sequentially with water and brine, dried over anhydrous sodium sulfate, and finally the solvent was evaporated under vacuum to afford the target product 2-((6-chloropyridin-2-yl)amino)ethanol (2.3 g, 99% yield) as a white solid.

[References]

[1] Patent: WO2008/62182, 2008, A1. Location in patent: Page/Page column 128
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