4-Amino-1-n-butoxycarbonyl-4-methyl-piperidine

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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:214.31
EINECS:674-596-1
Product Categories:
Mol File:343788-69-2.mol
4-Amino-1-n-butoxycarbonyl-4-methyl-piperidine Structure
4-Amino-1-n-butoxycarbonyl-4-methyl-piperidine Chemical Properties
Boiling point 283℃
density 1.017
Fp 125℃
storage temp. 2-8°C(protect from light)
pka9.77±0.20(Predicted)
AppearanceColorless to light yellow Solid-Liquid Mixture
Safety Information
HS Code 29333990
MSDS Information
4-Amino-1-n-butoxycarbonyl-4-methyl-piperidine Usage And Synthesis
Chemical PropertiesWhite powder
Synthesis
4-BENZYLOXY-CARBONYL-AMINO-1-N-BUTOXY-CARBONYL-4-METHYL PIPERIDINE

236406-14-7

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

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
Tag:4-Amino-1-n-butoxycarbonyl-4-methyl-piperidine(343788-69-2) Related Product Information
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