Basic information Safety Supplier Related

4-AMINO-1-N-BUTOXYCARBONYL-4-METHYL-PIPERIDINE

Basic information Safety Supplier Related

4-AMINO-1-N-BUTOXYCARBONYL-4-METHYL-PIPERIDINE Basic information

Product Name:
4-AMINO-1-N-BUTOXYCARBONYL-4-METHYL-PIPERIDINE
Synonyms:
  • 4-Amino-1-Boc-4-methylpiperidine
  • 4-Amino-1-Boc-4-methylpip...
  • 1-Boc-4-AMino-4-Methylpiperidine
  • 1-Piperidinecarboxylic acid, 4-aMino-4-Methyl-, 1,1-diMethylethyl ester
  • 1-(tert-Butoxycarbonyl)-4-amino-4-methylpiperidine
  • N-Boc-4-amino-4-methylpiperidine
  • 4-AMino-4-Methyl-1-piperidinecarboxylic acid tert-butyl ester
  • butyl 4-aMino-4-Methylpiperidine-1-carboxylate
CAS:
343788-69-2
MF:
C11H22N2O2
MW:
214.3
EINECS:
674-596-1
Mol File:
343788-69-2.mol
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4-AMINO-1-N-BUTOXYCARBONYL-4-METHYL-PIPERIDINE Chemical Properties

Boiling point:
283℃
Density 
1.017
Flash point:
125℃
storage temp. 
2-8°C(protect from light)
pka
9.77±0.20(Predicted)
Appearance
Colorless to light yellow Solid-Liquid Mixture
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Safety Information

HS Code 
29333990
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4-AMINO-1-N-BUTOXYCARBONYL-4-METHYL-PIPERIDINE Usage And Synthesis

Chemical Properties

White powder

Synthesis

236406-14-7

343788-69-2

General procedure for the synthesis of tert-butyl 4-amino-4-methylpiperidine-1-carboxylate from the compound (CAS: 236406-14-7): a mixture of the compound of formula LE (2.48 g, 7.11 mmol) with 10% palladium carbon (200 mg, Sigma-Aldrich) in methanol (20 mL) was subjected to an atmosphere of hydrogen at about 250 °C The reaction was stirred for 16 hours. Upon completion of the reaction, the Pd/C catalyst was removed by filtration and the filtrate was concentrated under reduced pressure to give 1.37 g of the compound of formula LF as a light-colored viscous oil (90.2% yield). The structure of tert-butyl 4-amino-4-methylpiperidine-1-carboxylate, compound of formula LF, was confirmed using 1H NMR. The 1H NMR data of compound LF were as follows: δH (400 MHz, CDCl3): 3.47-3.49 (4H, m), 1.47-1.61 (4H, m), 1.46 (9H, s), 1.31-1.42 (2H, m), 1.15 (3H, s).

References

[1] Patent: WO2008/89201, 2008, A2. Location in patent: Page/Page column 234-235
[2] Journal of Medicinal Chemistry, 2012, vol. 55, # 12, p. 5901 - 5921
[3] Patent: WO2006/38006, 2006, A2. Location in patent: Page/Page column 26-27
[4] Patent: WO2009/116067, 2009, A2. Location in patent: Page/Page column 139

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