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142896-15-9

142896-15-9 Structure

142896-15-9 Structure
IdentificationBack Directory
[Name]

2,6-DIMETHYLPYRIDINE-4-CARBOXYLIC ACID METHYL ESTER
[CAS]

142896-15-9
[Synonyms]

Methyl 2,6-diMethylisonicotinate
6-diMethylpyridine-4-carboxylate
Methyl 2,6-diMethylpyridine-4-carboxylate
2,6-Dimethyl-isonicotinic acid methyl ester
2,6-DIMETHYLPYRIDINE-4-CARBOXYLIC ACID METHYL ESTER
4-Pyridinecarboxylic acid, 2,6-diMethyl-, Methyl ester
Methyl 2,6-dimethylpyridine-4-carboxylate, 2,6-Dimethyl-4-(methoxycarbonyl)pyridine
[Molecular Formula]

C9H11NO2
[MDL Number]

MFCD11656351
[MOL File]

142896-15-9.mol
[Molecular Weight]

165.19
Chemical PropertiesBack Directory
[Melting point ]

45 °C
[Boiling point ]

238.1±35.0 °C(Predicted)
[density ]

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

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

4.55±0.10(Predicted)
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H315-H319-H335
[Precautionary statements ]

P271-P280
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

2,6-DIMETHYLPYRIDINE-4-CARBOXYLIC ACID METHYL ESTER(142896-15-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

METHYL 2,6-DICHLOROISONICOTINATE

42521-09-5

DIMETHYLZINC

544-97-8

2,6-DIMETHYLPYRIDINE-4-CARBOXYLIC ACID METHYL ESTER

142896-15-9

A mixture of methyl 2,6-dichloropyridine-4-carboxylate (2.00 g), dimethylzinc (2N toluene solution, 14.6 mL, 3.0 eq.), and PdCl2(dppf)2 (400 mg, 0.05 eq.) in dioxane (50 mL) was heated for 4 hr. at 80 °C under inert atmosphere. Upon completion of the reaction, the reaction mixture was cooled through an ice bath, quenched with water (100 mL) and filtered through a diatomaceous earth pad. The diatomaceous earth pad was rinsed with water and ethyl acetate (EtOAc). The filtrate was extracted with ethyl acetate (250 mL) and the organic layer was washed with brine (100 mL), dried over anhydrous magnesium sulfate (MgSO4) and concentrated. Purification by fast chromatography (methanol gradient in dichloromethane, 0 to 2%) afforded compound 99 (methyl 2,6-dimethylisonicotinate) as an orange oil in 96% yield.1H-NMR (400 MHz, DMSO): δ 2.51 (s, 6H, 2×CH3), 3.88 (s, 3H, O-CH3), 7.51 (s, 2H, Ar). Mass spectrum (M+H)+ m/z = 166.1.

[References]

[1] Patent: EP2666775, 2013, A1. Location in patent: Paragraph 0390
[2] Patent: WO2013/174822, 2013, A1. Location in patent: Page/Page column 137
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