ChemicalBook--->CAS DataBase List--->27225-00-9

27225-00-9

27225-00-9 Structure

27225-00-9 Structure
IdentificationBack Directory
[Name]

[2,7]NAPHTHYRIDIN-1-YLAMINE
[CAS]

27225-00-9
[Synonyms]

2,7phthyridin-1-ylamine
2,7-Naphthyridin-1-amine
1-Amino-2,7-naphthyridine
[2,7]NAPHTHYRIDIN-1-YLAMINE
[Molecular Formula]

C8H7N3
[MDL Number]

MFCD11506147
[MOL File]

27225-00-9.mol
[Molecular Weight]

145.16
Chemical PropertiesBack Directory
[Boiling point ]

363.7±27.0 °C(Predicted)
[density ]

1.292±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C(protect from light)
[pka]

5.54±0.30(Predicted)
[Appearance]

White to light yellow Solid
Safety DataBack Directory
[HS Code ]

2933998090
Spectrum DetailBack Directory
[Spectrum Detail]

[2,7]NAPHTHYRIDIN-1-YLAMINE(27225-00-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

4-[(E)-2-(dimethylamino)ethenyl]pyridine-3-carbonitrile

67988-51-6

[2,7]NAPHTHYRIDIN-1-YLAMINE

27225-00-9

To 4-((E)-2-dimethylamino vinyl) nicotinonitrile (253 g) was added ammonium formate (810 g) followed by acetic acid (300 mL) in a 4 L reaction vessel. The reaction mixture was heated to reflux at 115°C for 20 hours. Upon completion of the reaction, it was cooled to room temperature, diluted with the addition of water (5 L) and extracted several times with dichloromethane (0.5 L x 10). After combining the organic phases, the pH of the aqueous phase was adjusted with sodium hydroxide (160 g) to 10. Subsequently, the aqueous phase was extracted with methyl tert-butyl ether, and the organic phase was separated and dried with anhydrous sodium sulfate. The solvent was removed by concentration under reduced pressure, and after drying, 2,7-naphthyridin-1-amine (59 g) was obtained with a molecular weight of 145.16 g/mol (M+H measured value of 146), and the NMR spectrum was consistent with the target product.

[References]

[1] Patent: US2015/252041, 2015, A1. Location in patent: Paragraph 0166
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