ChemicalBook--->CAS DataBase List--->5810-56-0

5810-56-0

5810-56-0 Structure

5810-56-0 Structure
IdentificationMore
[Name]

4-ACETAMIDOPIPERIDINE
[CAS]

5810-56-0
[Synonyms]

4-ACETAMIDOPIPERIDINE
N-PIPERIDIN-4-YL-ACETAMIDE
4-Acetylamino-piperidine
4-ACETYLAMINO-PIPERIDINE >98%
[Molecular Formula]

C7H14N2O
[MDL Number]

MFCD05254805
[Molecular Weight]

142.2
[MOL File]

5810-56-0.mol
Chemical PropertiesBack Directory
[Melting point ]

141 °C
[Boiling point ]

318.5±31.0 °C(Predicted)
[density ]

1.02
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[solubility ]

soluble in Methanol
[form ]

powder to crystal
[pka]

15.96±0.20(Predicted)
[color ]

White to Almost white
[CAS DataBase Reference]

5810-56-0(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S37:Wear suitable gloves .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
[HS Code ]

29333990
Spectrum DetailBack Directory
[Spectrum Detail]

4-ACETAMIDOPIPERIDINE(5810-56-0)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

4-Acetamidopiperidine(5810-56-0)
[TCI AMERICA]

4-Acetamidopiperidine,>98.0%(T)(5810-56-0)
Hazard InformationBack Directory
[Synthesis]

4-ACETAMIDO-1-BENZYLPIPERIDINE

50534-23-1

4-ACETAMIDOPIPERIDINE

5810-56-0

General procedure for the synthesis of 4-acetamido-piperidine from 4-acetamido-1-benzylpiperidine: preparation of intermediate 40: N-piperidin-4-yl-acetamide (method step 10). Pd-C (350 mg) was added to a solution of N-(1-benzyl-piperidin-4-yl)-acetamide (intermediate 39) (2.3 g, 10.0 mmol) in EtOH (35 mL) and HCl (1 M, 5 mL), and the mixture was stirred for 5 hr under hydrogen atmosphere. Upon completion of the reaction, the catalyst was removed by filtration through diatomaceous earth followed by washing with EtOH and then water. The filtrate was concentrated under vacuum and the product was purified by column chromatography using a methanol solution of dichloromethane/7M NH3 (100:0 to 80:20) as eluent to give the intermediate 40 (0.92 g, 65% yield). Since the compound could not be detected by HPLC-MS, its structure was confirmed by NMR.

[References]

[1] Bioorganic and Medicinal Chemistry Letters, 2003, vol. 13, # 14, p. 2303 - 2306
[2] Organic Process Research and Development, 2012, vol. 16, # 3, p. 470 - 483
[3] Patent: US2012/214798, 2012, A1
[4] Patent: US2005/43298, 2005, A1. Location in patent: Page/Page column 35
[5] Patent: US2005/197333, 2005, A1. Location in patent: Page/Page column 39-40
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