ChemicalBook--->CAS DataBase List--->169750-96-3

169750-96-3

169750-96-3 Structure

169750-96-3 Structure
IdentificationBack Directory
[Name]

3-(Boc-amino)-3-methylpip...
[CAS]

169750-96-3
[Synonyms]

3-(Boc-amino)-3-methylpip...
3-(Boc-aMino)-3-Methylpiperidine
3-Amino-3-methylpiperidine, 3-BOC protected
tert-Butyl 3-methylpiperidin-3-yl-carbamate
tert-butyl n-(3-methylpiperidin-3-yl)carbamate
(3-Methyl-piperidin-3-yl)-carbamic acid tert-butyl ester
(3-Methyl-3-piperidinyl)carbamic acid 1,1-dimethylethyl ester
Carbamic acid, N-(3-methyl-3-piperidinyl)-, 1,1-dimethylethyl ester
tert-Butyl (3-methylpiperidin-3-yl)carbamate, 3-[(tert-Butoxycarbonyl)amino]-3-methylpiperidine
[Molecular Formula]

C11H22N2O2
[MDL Number]

MFCD13194151
[MOL File]

169750-96-3.mol
[Molecular Weight]

214.3
Chemical PropertiesBack Directory
[Boiling point ]

308.4±31.0 °C(Predicted)
[density ]

1.01±0.1 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,2-8°C
[pka]

12?+-.0.20(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

3-(Boc-amino)-3-methylpip...(169750-96-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

1-Piperidinecarboxylic acid, 3-[[(1,1-dimethylethoxy)carbonyl]amino]-3-methyl-, phenylmethyl ester

1196506-86-1

3-(Boc-amino)-3-methylpip...

169750-96-3

General procedure for the synthesis of tert-butyl (3-methylpiperidin-3-yl)carbamate from the compound (CAS:1196506-86-1): benzyl 3-((tert-butoxycarbonyl)amino)-3-methylpiperidine-1-carboxylate (78 mg, 0.22 mmol, prepared according to the method described in WO09/140320) was dissolved in EtOH (5 mL) , which was degassed by bubbling N2 (g) into the solution for 10 min. Pd/C (10 wt%, 24 mg, 0.022 mmol) was added. A gas bladder attached to a three-way cork filled with H2 was connected to the flask. The flask was evacuated and backfilled with H2 (repeated 3 times). The mixture was stirred at room temperature for 2 hours. Degassing was again carried out by bubbling N2 (g) into the solution for 10 min, followed by filtration through diatomaceous earth. The filtrate was concentrated to give racemic-tert-butyl (3-methylpiperidin-3-yl) carbamate (42 mg, 0.20 mmol, 88% yield) as a clear, colorless oil.MS (ESI, cationic) m/z: 215.1 (M + 1).

[References]

[1] Patent: WO2012/148775, 2012, A1. Location in patent: Page/Page column 124; 125
[2] Patent: WO2009/140320, 2009, A1. Location in patent: Page/Page column 73
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