ChemicalBook--->CAS DataBase List--->1073182-59-8

1073182-59-8

1073182-59-8 Structure

1073182-59-8 Structure
IdentificationBack Directory
[Name]

Methyl 5-aMino-2-chloropyridine-4-carboxylate
[CAS]

1073182-59-8
[Synonyms]

Methyl 5-amino-2-chloroisonicotinate 95%
Methyl 5-aMino-2-chloropyridine-4-carboxylate
4-Pyridinecarboxylic acid, 5-amino-2-chloro-, methyl ester
Methyl 5-amino-2-chloropyridine-4-carboxylate, 5-Amino-2-chloro-4-(methoxycarbonyl)pyridine
[Molecular Formula]

C7H7ClN2O2
[MDL Number]

MFCD11848213
[MOL File]

1073182-59-8.mol
[Molecular Weight]

186.6
Chemical PropertiesBack Directory
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[Appearance]

Light yellow to yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332
[Precautionary statements ]

P261-P271-P280
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

Methyl 5-amino-2-chloroisonicotinate(1073182-59-8)1HNMR
Hazard InformationBack Directory
[Synthesis]

Methanol

67-56-1

5-[(TERT-BUTOXYCARBONYL)AMINO]-2-CHLOROISONICOTINIC ACID

171178-46-4

Methyl 5-amino-2-chloroisonicotinate

1073182-59-8

To a stirred solution of 5-tert-butoxycarbonylamino-2-chloroisonicotinic acid (crude, 8.0 g) in methanol (50 mL) was slowly added concentrated sulfuric acid (5.0 mL). The reaction mixture was heated to reflux and kept at this condition for the reaction overnight. Upon completion of the reaction, the mixture was cooled to room temperature and subsequently concentrated under reduced pressure to remove the solvent. The concentrated residue was diluted with an appropriate amount of water and then neutralized with saturated sodium bicarbonate solution to pH=8. The neutralized aqueous phase was extracted with ethyl acetate (100 mL x2). The organic phases were combined and washed with saturated brine (50 mL), followed by drying with anhydrous sodium sulfate and filtration. The filtrate was evaporated to dryness under reduced pressure and the resulting crude product was purified by silica gel column chromatography.

[References]

[1] Patent: WO2015/200534, A2. Location in patent: Paragraph 00480
[1] Patent: , 2015, . Location in patent: Paragraph 00480
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