ChemicalBook--->CAS DataBase List--->1314353-68-8

1314353-68-8

1314353-68-8 Structure

1314353-68-8 Structure
IdentificationBack Directory
[Name]

5-cyclopropylpyridin-3-aMine
[CAS]

1314353-68-8
[Synonyms]

5-cyclopropylpyridin-3-aMine
3-Pyridinamine, 5-cyclopropyl-
[Molecular Formula]

C8H10N2
[MDL Number]

MFCD19543987
[MOL File]

1314353-68-8.mol
[Molecular Weight]

134.18
Chemical PropertiesBack Directory
[Boiling point ]

308.6±30.0 °C(Predicted)
[density ]

1.188±0.06 g/cm3(Predicted)
[storage temp. ]

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

6.54±0.20(Predicted)
[Appearance]

Light yellow to yellow Solid
Safety DataBack Directory
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

5-cyclopropylpyridin-3-aMine(1314353-68-8)1HNMR
Hazard InformationBack Directory
[Synthesis]

3-Amino-5-bromopyridine

13535-01-8

Cyclopropylboronic acid

411235-57-9

5-cyclopropylpyridin-3-aMine

1314353-68-8

General procedure for the synthesis of 5-cyclopropylpyridin-3-amine from 5-bromo-3-aminopyridine and cyclopropylboronic acid: To a solution of 5-bromopyridin-3-amine (4.75 g, 27.45 mmol) in dioxane (45 mL) was added cyclopropylboronic acid (4.75 g, 55.30 mmol), cesium carbonate (Cs2CO3, 28 g, 85.67 mmol) in sequence , tetrakis(triphenylphosphine)palladium (1.66 g, 1.44 mmol), and water (5 mL), and mixed with stirring at room temperature. The reaction mixture was heated to 100 °C with continuous stirring for 15 hours. After the reaction was completed, it was cooled to room temperature and the reaction mixture was diluted with water (200 mL). The mixture was extracted with ethyl acetate (500 mL x 3) and the organic phases were combined. The organic phase was washed with saturated brine and dried over anhydrous sodium sulfate (Na2SO4). The solvent was removed by concentration under reduced pressure and the residue was purified by fast column chromatography using hexane/ethyl acetate (0% to 100% gradient) as eluent to afford 5-cyclopropylpyridin-3-amine as a light brown oil (2.08 g, 56% yield). Mass spectrum (MS): m/z = 135.0 [M + H]+.

[References]

[1] Patent: WO2017/106607, 2017, A1. Location in patent: Paragraph 00477
[2] Patent: EP2762476, 2014, A1. Location in patent: Paragraph 0174
[3] Patent: US2014/309225, 2014, A1. Location in patent: Paragraph 0700; 0701; 0702; 0703
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