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ChemicalBook CAS DataBase List tert-butyl(S)-4-(6-aminopyridin-3-yl)-3-methylpiperazine-1-carboxylate
1433849-58-1

tert-butyl(S)-4-(6-aminopyridin-3-yl)-3-methylpiperazine-1-carboxylate synthesis

4synthesis methods
tert-butyl (S)-3-methyl-4-(6-nitropyridin-3-yl)piperazine-1-carboxylate

1433849-53-6
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tert-butyl(S)-4-(6-aminopyridin-3-yl)-3-methylpiperazine-1-carboxylate

1433849-58-1
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Yield:1433849-58-1 96%

Reaction Conditions:

with Pd/C;hydrogen in ethanol at 20; for 16 h;Inert atmosphere;

Steps:

105.b (3S)-tert-Butyl 4-(6-Aminopyridin-3-yl)-3-methylpiperazine-1-carboxylate 105b

Example 105b
(3S)-tert-Butyl 4-(6-Aminopyridin-3-yl)-3-methylpiperazine-1-carboxylate 105b
A 500-mL bottle was purged with nitrogen and charged with 105a (5.8 g, 18 mmol), 10% palladium on carbon (50% wet, 2.0 g) and ethanol (200 mL).
It was evacuated, charged with hydrogen gas, and stirred for 16 h at room temperature.
The hydrogen was then removed in vacuo and replaced with nitrogen.
The catalyst was removed by filtration through a pad of CELITE and the filtrate concentrated under reduced pressure to afford 105b as a brown solid (4.9 g, 96%). LCMS: [M+H]+ 293

References:

US2013/116246,2013,A1 Location in patent:Paragraph 0255; 0256

147081-29-6 Synthesis
(S)-1-Boc-3-methylpiperazine

147081-29-6
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tert-butyl(S)-4-(6-aminopyridin-3-yl)-3-methylpiperazine-1-carboxylate

1433849-58-1
18 suppliers
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