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912369-42-7

912369-42-7 Structure

912369-42-7 Structure
IdentificationBack Directory
[Name]

Methyl 3-(tert-butoxycarbonylamino)picolinate
[CAS]

912369-42-7
[Synonyms]

Methyl 3-(BOC-amino)picolinate
Methyl 3-(tert-butoxycarbonyl)picolinate
Methyl 3-(Boc-amino)pyridine-2-carboxylate
Methyl 3-(tert-butoxycarbonylamino)picolinate
methyl 3-{[(tert-butoxy)carbonyl]amino}pyridine-2-carboxylate
3-tert-Butoxycarbonylamino-pyridine-2-carboxylic acid methyl ester
Methyl 3-[(2-methylpropan-2-yl)oxycarbonylamino]pyridine-2-carboxylate
2-Pyridinecarboxylic acid, 3-[[(1,1-dimethylethoxy)carbonyl]amino]-, methyl ester
[Molecular Formula]

C12H16N2O4
[MDL Number]

MFCD12026422
[MOL File]

912369-42-7.mol
[Molecular Weight]

252.27
Chemical PropertiesBack Directory
[Melting point ]

94 °C(Solv: hexane (110-54-3))
[Boiling point ]

339.9±27.0 °C(Predicted)
[density ]

1.203±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,2-8°C
[pka]

12.32±0.70(Predicted)
[Appearance]

White to off-white Solid
Spectrum DetailBack Directory
[Spectrum Detail]

Methyl 3-(tert-butoxycarbonylamino)picolinate(912369-42-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

quinolinic acid, 2-methyl ester

24195-07-1

tert-Butanol

75-65-0

Methyl 3-(tert-butoxycarbonylamino)picolinate

912369-42-7

2-(Methoxycarbonyl)pyridine-3-carboxylic acid (3 g, 16.57 mmol) was dissolved in 50 mL of tert-butanol and triethylamine (4 mL) was added. After stirring at room temperature for 5 minutes, diphenylphosphoryl azide (3.6 mL, 16.57 mmol) was added and the reaction mixture was refluxed for 3 hours. Upon completion of the reaction, the mixture was concentrated and the residue was purified by fast column chromatography (silica gel) with ethyl acetate/cyclohexane (20% to 50% gradient) as eluent. The fraction containing the target product was collected and concentrated in vacuum to afford methyl 3-{[(tert-butoxy)carbonyl]amino}pyridine-2-carboxylate (1.6 g, 38.5% yield).

[References]

[1] Patent: WO2016/196776, 2016, A2. Location in patent: Paragraph 00765
[2] Journal of Medicinal Chemistry, 2009, vol. 52, # 9, p. 2754 - 2761
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