ChemicalBook--->CAS DataBase List--->70298-88-3

70298-88-3

70298-88-3 Structure

70298-88-3 Structure
IdentificationBack Directory
[Name]

2,2-DIMETHYL-N-PYRIDIN-3-YL-PROPIONAMIDE
[CAS]

70298-88-3
[Synonyms]

Zinc04352664
N-(3-Pyridyl)pivalaMide
3-(Pivaloylamino)pyridine
N-(Pyridin-3-yl)pivalamide
N-(3-Pyridyl)pivalamide>
2,2-diMethyl-N-pyridin-3-ylpropanaMide
2,2-Dimethyl-N-pyridine-3yl-propionamide
2,2-Dimehtyl-N-pyridin-3-yl-propionamide
Propanamide, 2,2-dimethyl-N-3-pyridinyl-
2,2-DIMETHYL-N-PYRIDIN-3-YL-PROPIONAMIDE
2,2-DiMethyl-N-(3-pyridyl)propionaMide, 98%
[EINECS(EC#)]

1312995-182-4
[Molecular Formula]

C10H14N2O
[MDL Number]

MFCD00996243
[MOL File]

70298-88-3.mol
[Molecular Weight]

178.23
Chemical PropertiesBack Directory
[Melting point ]

129-131℃
[Boiling point ]

337.5±15.0 °C(Predicted)
[density ]

1.078±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

soluble in Methanol
[form ]

powder to crystal
[pka]

14.19±0.70(Predicted)
[color ]

White to Light yellow to Light orange
Safety DataBack Directory
[Hazard Codes ]

Xi,Xn
[Risk Statements ]

22
[WGK Germany ]

3
[HazardClass ]

IRRITANT
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

2,2-DIMETHYL-N-PYRIDIN-3-YL-PROPIONAMIDE(70298-88-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

3-Aminopyridine

462-08-8

Pivaloyl chloride

3282-30-2

2,2-DIMETHYL-N-PYRIDIN-3-YL-PROPIONAMIDE

70298-88-3

In a dry three-necked flask, 3-aminopyridine (20.0 g, 212.5 mmol), 4-dimethylaminopyridine (DMAP) (0.3 g, 2.1 mmol) and pyridine (33.6 g, 425.0 mmol) were dissolved in anhydrous dichloromethane (200 mL). Valeroyl chloride (28.2 g, 233.7 mmol) was added slowly and dropwise under cooling in an ice bath. The reaction mixture was kept stirred at 0 °C for 2 hours. After completion of the reaction, the reaction solution was slowly poured into ice water and the reaction was quenched with 1N hydrochloric acid solution. Subsequently, the mixture was extracted with dichloromethane (250 mL × 3), the organic phases were combined and washed with saturated saline (200 mL × 1). Finally, the solvent was removed by distillation under reduced pressure to afford 3-pivalamido pyridine (36.2 g) as a white solid in 95.5% yield.

[References]

[1] Synthesis, 1982, # 6, p. 499 - 500
[2] Tetrahedron, 2009, vol. 65, # 18, p. 3668 - 3672
[3] Patent: CN107382839, 2017, A. Location in patent: Paragraph 0005; 0012-0013; 0020-0021; 0028-0029; 0036-0037
[4] Patent: WO2014/198844, 2014, A1. Location in patent: Page/Page column 15; 16
[5] Patent: WO2014/198848, 2014, A2. Location in patent: Page/Page column 14; 15
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