ChemicalBook--->CAS DataBase List--->1209646-17-2

1209646-17-2

1209646-17-2 Structure

1209646-17-2 Structure
IdentificationBack Directory
[Name]

5-(4-(tert-butoxycarbonyl)piperazin-1-yl)pyrazine-2-carboxylic acid
[CAS]

1209646-17-2
[Synonyms]

5-(4-(tert-Butoxycarbonyl)
5-(4-(tert-butoxycarbonyl)piperazin-1-yl)pyrazine-2-carboxylic acid
2-Pyrazinecarboxylic acid, 5-[4-[(1,1-dimethylethoxy)carbonyl]-1-piperazinyl]-
[Molecular Formula]

C14H20N4O4
[MDL Number]

MFCD12923092
[MOL File]

1209646-17-2.mol
[Molecular Weight]

308.33
Chemical PropertiesBack Directory
[storage temp. ]

2-8°C
[Appearance]

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

5-(4-(tert-butoxycarbonyl)piperazin-1-yl)pyrazine-2-carboxylic acid(1209646-17-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

methyl 5-(4-(tert-butoxycarbonyl)piperazin-1-yl)pyrazine-2-carboxylate

1215626-40-6

5-(4-(tert-butoxycarbonyl)piperazin-1-yl)pyrazine-2-carboxylic acid

1209646-17-2

Methyl 5-(4-(tert-butoxycarbonyl)piperazin-1-yl)pyrazine-2-carboxylate (2 g, crude) was used as a raw material, which was dissolved in a mixed solvent of ethanol (5 mL) and tetrahydrofuran (5 mL), followed by the addition of 2N sodium hydroxide solution (5 mL). The reaction mixture was stirred at 60°C for 2 hours. Upon completion of the reaction, the pH was adjusted to 1 with dilute hydrochloric acid and subsequently extracted with ethyl acetate. The organic phase was concentrated to give the pink solid product 5-(4-(tert-butoxycarbonyl)piperazin-1-yl)pyrazine-2-carboxylic acid (300 mg, 15% yield, two steps).

[References]

[1] Patent: WO2012/24150, 2012, A1. Location in patent: Page/Page column 130
[2] Patent: WO2012/27322, 2012, A1. Location in patent: Page/Page column 102
[3] Patent: WO2012/40139, 2012, A1. Location in patent: Page/Page column 100
[4] Patent: US2013/195879, 2013, A1. Location in patent: Paragraph 0266
[5] Patent: US2018/141923, 2018, A1. Location in patent: Paragraph 0474; 0477; 0478
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