Identification | Back 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 Properties | Back 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 |
Hazard Information | Back Directory | [Synthesis]
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 |
|
Company Name: |
Energy Chemical
|
Tel: |
021-021-58432009 400-005-6266 |
Website: |
http://www.energy-chemical.com |
|