ChemicalBook--->CAS DataBase List--->710972-40-0

710972-40-0

710972-40-0 Structure

710972-40-0 Structure
IdentificationBack Directory
[Name]

4-(2-METHOXYETHYLAMINO)PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
[CAS]

710972-40-0
[Synonyms]

1-Boc-4-(2-methoxyethylamino)piperidine
N-Boc-4-(2-methoxyethylamino)-piperidine
1-Boc-N-(2-methoxyethyl)piperidin-4-amine
TERT-BUTYL 4-[(2-METHOXYETHYL)AMINO]PIPERIDINE-1-CARBOXYLATE
4-(2-methoxyethylamino)piperidine-1-carbpxylic acid tert-butyl ester
4-(2-METHOXYETHYLAMINO)PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
4-(2-methoxyethylamino)-1-piperidinecarboxylic acid tert-butyl ester
1,1-diMethylethyl 4-([2-(Methyloxy)ethyl]aMino)-1-piperidinecarboxylate
4-(2-METHOXYETHYLAMINO)PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER, 95+%
[Molecular Formula]

C13H26N2O3
[MDL Number]

MFCD06656630
[MOL File]

710972-40-0.mol
[Molecular Weight]

258.36
Chemical PropertiesBack Directory
[Boiling point ]

337.6±32.0 °C(Predicted)
[density ]

1.03±0.1 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[pka]

9.01±0.20(Predicted)
[Appearance]

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

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Hazard Codes ]

Xn
[Risk Statements ]

22
Spectrum DetailBack Directory
[Spectrum Detail]

4-(2-METHOXYETHYLAMINO)PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER(710972-40-0)1HNMR
Hazard InformationBack Directory
[Synthesis]

N-(tert-Butoxycarbonyl)-4-piperidone

79099-07-3

2-METHOXYETHYLAMINE

109-85-3

4-(2-METHOXYETHYLAMINO)PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER

710972-40-0

To a solution of N-tert-butoxycarbonyl-4-piperidone (1 g, 5.0 mmol) in methanol (20 mL) was sequentially added acetic acid (0.3 mL, 5.0 mmol), 2-methoxyethylamine (0.44 mL, 5.0 mmol), and sodium cyanoborohydride (346 mg, 5.5 mmol). The reaction mixture was stirred at 25°C for 12 hours. After completion of the reaction, the reaction solution was diluted with aqueous sodium carbonate and extracted with ethyl acetate several times. The organic phases were combined, concentrated and purified by silica gel column chromatography (eluent: dichloromethane/methanol, 0-10% gradient) to afford tert-butyl 4-(2-methoxyethylamino)piperidine-1-carboxylate (1.2 g, 93%) as a yellow oil.LC/MS (ES) m/e 259 (M+H)+.

[References]

[1] Patent: WO2007/16610, 2007, A2. Location in patent: Page/Page column 49; 50
[2] Patent: WO2017/21730, 2017, A1. Location in patent: Page/Page column 59
[3] Patent: WO2006/46031, 2006, A1. Location in patent: Page/Page column 56; 58
[4] Patent: CN107814792, 2018, A. Location in patent: Paragraph 0223; 0224
[5] Patent: WO2007/122410, 2007, A1. Location in patent: Page/Page column 94-95; 101-102
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