ChemicalBook--->CAS DataBase List--->603310-75-4

603310-75-4

603310-75-4 Structure

603310-75-4 Structure
IdentificationBack Directory
[Name]

5-(1-Methylethyl)-2-pyridinamine
[CAS]

603310-75-4
[Synonyms]

2-AMino-5-isopropylpyridine
5-(propan-2-yl)pyridin-2-aMine
(5-Isopropylpyridin-2-yl)amine
2-amino-5-(propan-2-yl)pyridine
5-(1-Methylethyl)-2-Pyridinamine
2-PYRIDINAMINE, 5-(1-METHYLETHYL)-
2-Pyridinamine,5-(1-methylethyl)-(9CI)
[EINECS(EC#)]

200-258-5
[Molecular Formula]

C8H12N2
[MDL Number]

MFCD08460246
[MOL File]

603310-75-4.mol
[Molecular Weight]

136.19
Chemical PropertiesBack Directory
[Boiling point ]

253 ºC
[density ]

1.008
[Fp ]

130 ºC
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[pka]

6.95±0.13(Predicted)
[Appearance]

Light yellow to brown Solid-liquid mixture
Questions And AnswerBack Directory
[Uses]

5-Isopropylpyridine-2-amine can be used as a pharmaceutical synthesis intermediate.
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[RIDADR ]

UN2810
[HazardClass ]

6.1
Spectrum DetailBack Directory
[Spectrum Detail]

5-(1-Methylethyl)-2-pyridinamine(603310-75-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-Nitro-5-(prop-1-en-2-yl)pyridine

1135437-90-9

5-(1-Methylethyl)-2-pyridinamine

603310-75-4

Step B: Synthesis of 5-isopropylpyridin-2-amine as an intermediate; [0209] A mixture of 2-nitro-5-(prop-1-en-2-yl)pyridine (0.104 g, 0.63 mmol) with 10% palladium-carbon catalyst (0.011 g, 10 wt%) in ethanol (10 mL) was subjected to a hydrogen atmosphere and stirred at atmospheric pressure for overnight reaction. Upon completion of the reaction, the catalyst was removed by diatomaceous earth filtration and the filtrate was concentrated under reduced pressure to give 5-isopropylpyridin-2-amine (0.120 g, 139% yield) as an oily product. Its structure was confirmed by 1H NMR (500 MHz, CDCl3): δ 7.68 (d, J = 8.1 Hz, 1H), 7.51 (s, 1H), 7.48 (s, 2H), 7.14 (d, J = 9.1 Hz, 1H), 3.45-3.42 (m, 1H), 1.38 (d, J = 8.6 Hz, 6H); ESI MS m/z 137 [M + H]+.

[References]

[1] Patent: WO2009/42907, 2009, A1. Location in patent: Page/Page column 83
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