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

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5-(4-(tert-butoxycarbonyl)piperazin-1-yl)pyrazine-2-carboxylic acid Basic information
Product Name:5-(4-(tert-butoxycarbonyl)piperazin-1-yl)pyrazine-2-carboxylic acid
Synonyms:5-(4-(tert-butoxycarbonyl)piperazin-1-yl)pyrazine-2-carboxylic acid;5-(4-(tert-Butoxycarbonyl);2-Pyrazinecarboxylic acid, 5-[4-[(1,1-dimethylethoxy)carbonyl]-1-piperazinyl]-;5-(4-Boc-1-piperazinyl)pyrazine-2-carboxylic Acid
CAS:1209646-17-2
MF:C14H20N4O4
MW:308.33
EINECS:
Product Categories:
Mol File:1209646-17-2.mol
5-(4-(tert-butoxycarbonyl)piperazin-1-yl)pyrazine-2-carboxylic acid Structure
5-(4-(tert-butoxycarbonyl)piperazin-1-yl)pyrazine-2-carboxylic acid Chemical Properties
storage temp. 2-8°C
AppearanceWhite to off-white Solid
Safety Information
MSDS Information
5-(4-(tert-butoxycarbonyl)piperazin-1-yl)pyrazine-2-carboxylic acid Usage And Synthesis
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
5-(4-(tert-butoxycarbonyl)piperazin-1-yl)pyrazine-2-carboxylic acid Preparation Products And Raw materials
Raw materialsmethyl 5-(4-(tert-butoxycarbonyl)piperazin-1-yl)pyrazine-2-carboxylate-->Sodium hydroxide-->Ethanol-->Tetrahydrofuran
Tag:5-(4-(tert-butoxycarbonyl)piperazin-1-yl)pyrazine-2-carboxylic acid(1209646-17-2) Related Product Information
Methyl 6-(4-(tert-butoxycarbonyl)piperazin-1-yl)pyrazine-2-carboxylate tert-Butyl 4-(3-aMinopyrazin-2-yl)piperazine-1-carboxylate 6'-CHLORO-2,3,5,6-TETRAHYDRO-[1,2']BIPYRAZINYL-4-CARBOXYLIC ACID TERT-BUTYL ESTER 2-Pyrazinecarboxylic acid, 5-(1-piperazinyl)- methyl 5-(4-(tert-butoxycarbonyl)piperazin-1-yl)pyrazine-2-carboxylate 1-Piperazinecarboxylic acid, 4-[6-(hydroxymethyl)-2-pyrazinyl]-, 1,1-dimethylethyl ester