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343788-69-2

343788-69-2 Structure

343788-69-2 Structure
IdentificationBack Directory
[Name]

4-AMINO-1-N-BUTOXYCARBONYL-4-METHYL-PIPERIDINE
[CAS]

343788-69-2
[Synonyms]

4-Amino-1-Boc-4-methylpip...
TERT-BUTYL-4-AMINO-4-METHYLPIP
1-Boc-4-AMino-4-Methylpiperidine
4-Amino-1-Boc-4-methylpiperidine
N-Boc-4-amino-4-methylpiperidine
1-BOC-4-AMINO-4-METHYL PIPERADINE
4-AMINO-4-METHYL-N-BOC-PIPERIDINE
4-AMINO-4-METHYL-1-BOC-PIPERIDINE
4-Amino-1-N-boc-4-methyl-piperidine
butyl 4-aMino-4-Methylpiperidine-1-carboxylate
4-AMINO-1-N-BUTOXYCARBONYL-4-METHYL-PIPERIDINE
1-(tert-Butoxycarbonyl)-4-amino-4-methylpiperidine
TERT-BUTYL 4-AMINO-4-METHYLPIPERIDINE-1-CARBOXYLATE
4-AMINO-1-N-TERT-BUTYLOXYCARBONYL-4-METHYL-PIPERIDINE
4-AMino-4-Methyl-1-piperidinecarboxylic acid tert-butyl ester
1-Piperidinecarboxylic acid, 4-aMino-4-Methyl-, 1,1-diMethylethyl ester
[EINECS(EC#)]

674-596-1
[Molecular Formula]

C11H22N2O2
[MDL Number]

MFCD03411925
[MOL File]

343788-69-2.mol
[Molecular Weight]

214.3
Chemical PropertiesBack Directory
[Boiling point ]

283℃
[density ]

1.017
[Fp ]

125℃
[storage temp. ]

Keep in dark place,Sealed in dry,2-8°C
[pka]

9.77±0.20(Predicted)
[Appearance]

Colorless to light yellow Solid-Liquid Mixture
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)Health Hazard (GHS08)Flame (GHS02)
GHS07,GHS08,GHS02
[Signal word ]

Danger
[Hazard statements ]

H315-H319-H341-H412-H225
[Precautionary statements ]

P501-P273-P202-P240-P210-P233-P201-P243-P241-P242-P264-P280-P370+P378-P308+P313-P337+P313-P305+P351+P338-P362+P364-P303+P361+P353-P332+P313-P403+P235-P405
[HS Code ]

29333990
Hazard InformationBack Directory
[Chemical Properties]

White 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
Spectrum DetailBack Directory
[Spectrum Detail]

4-AMINO-1-N-BUTOXYCARBONYL-4-METHYL-PIPERIDINE(343788-69-2)1HNMR
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