ChemicalBook--->CAS DataBase List--->295327-27-4

295327-27-4

295327-27-4 Structure

295327-27-4 Structure
IdentificationBack Directory
[Name]

ETHYL 2-(3-AMINOPYRIDIN-2-YL)ACETATE
[CAS]

295327-27-4
[Synonyms]

Ethyl (3-aminopyridin-2-yl)acetate
Ethyl 2-(3-aminopyridin-yl)acetate
Ethyl (3-amino-2-pyridinyl)acetate
ETHYL 2-(3-AMINOPYRIDIN-2-YL)ACETAT
ETHYL 2-(3-AMINOPYRIDIN-2-YL)ACETATE
3-Amino-2-pyridineacetic acid ethyl ester
2-Pyridineacetic acid, 3-aMino-, ethyl ester
Ethyl 2-(3-aminopyridin-2-yl)ethanoate, 3-Amino-2-(2-ethoxy-2-oxoethyl)pyridine
[Molecular Formula]

C9H12N2O2
[MDL Number]

MFCD11616148
[MOL File]

295327-27-4.mol
Chemical PropertiesBack Directory
[storage temp. ]

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

solid
[color ]

Yellow
Safety DataBack Directory
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

ETHYL 2-(3-AMINOPYRIDIN-2-YL)ACETATE(295327-27-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

ETHYL 2-(3-NITROPYRIDIN-2-YL)ACETATE

154078-83-8

ETHYL 2-(3-AMINOPYRIDIN-2-YL)ACETATE

295327-27-4

c) Synthesis of 2-(3-aminopyridin-2-yl)ethyl acetate: Pd/C (10%, 1.36 g) was added to a round-bottomed flask under nitrogen protection. Ethyl 2-(3-nitropyridin-2-yl)acetate (8.6 g, 0.041 mol) was dissolved in ethanol (200 mL) and subsequently added to the reaction vessel. The reaction system was placed under hydrogen atmosphere and the reaction was stirred at room temperature for 30 minutes. Upon completion of the reaction, the reaction mixture was filtered through diatomaceous earth and the filtrate was concentrated under vacuum to afford the brown solid product ethyl 2-(3-aminopyridin-2-yl)acetate (6.94 g, 94% yield).

[References]

[1] Patent: US6369086, 2002, B1
[2] Patent: US6369086, 2002, B1
[3] Patent: US6624171, 2003, B1
[4] Patent: US6350747, 2002, B1. Location in patent: Page column 72
[5] Bioorganic and Medicinal Chemistry Letters, 2004, vol. 14, # 4, p. 953 - 957
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