Basic information Safety Supplier Related

1-BENZYL-4-(N-BOC-AMINO) PIPERIDINE 98

Basic information Safety Supplier Related

1-BENZYL-4-(N-BOC-AMINO) PIPERIDINE 98 Basic information

Product Name:
1-BENZYL-4-(N-BOC-AMINO) PIPERIDINE 98
Synonyms:
  • 1-Benzyl-4-(N-Boc-amino)piperidine
  • (1-Benzyl-piperidin-4-yl)-carbamic acid tert-butyl ester
  • tert-butyl N-(1-benzylpiperidin-4-yl)carbamate
  • 4-Boc-aMino-1-benzylpiperidine
  • N-Benzyl-4-(N-Boc-aMino)piperidine
  • tert-Butyl 1-benzylpiperidin-4-ylcarbamate
  • 4-(N-Boc-aMino)-1-benzyl-piperidine
  • 1-BENZYL-4-(N-BOC-AMINO) PIPERIDINE 98
CAS:
73889-19-7
MF:
C17H26N2O2
MW:
290.4
Product Categories:
  • Building Blocks
  • Heterocyclic Building Blocks
  • Piperidines
  • Amines and Anilines
  • Heterocycles
Mol File:
73889-19-7.mol
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1-BENZYL-4-(N-BOC-AMINO) PIPERIDINE 98 Chemical Properties

Melting point:
122-125 °C(lit.)
Boiling point:
400.9±34.0 °C(Predicted)
Density 
1.07±0.1 g/cm3(Predicted)
storage temp. 
2-8°C
pka
12.35±0.20(Predicted)
Appearance
White to off-white Solid
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HS Code 
29333990
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1-BENZYL-4-(N-BOC-AMINO) PIPERIDINE 98 Usage And Synthesis

Chemical Properties

White powder

Synthesis

50541-93-0

24424-99-5

73889-19-7

General procedure for the synthesis of tert-butyl (1-benzylpiperidin-4-yl)carbamate from 4-amino-1-benzylpiperidine and di-tert-butyl dicarbonate: to an anhydrous solution of 4-amino-1-benzylpiperidine (1 mL, 933 mg, 4.9 mmol) in dichloromethane (20 mL) was added triethylamine (1 mL, 725 mg, 7.2 mmol) and di-tert-butyl dicarbonate ( 1.23 g, 5.6 mmol). The reaction mixture was stirred overnight at room temperature and then diluted with dichloromethane (20 mL). The organic layer was washed sequentially with saturated aqueous sodium bicarbonate (10 mL) and saturated saline (10 mL), dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to give tert-butyl (1-benzylpiperidin-4-yl)carbamate (1.42 g, quantitative yield) as a white solid.

References

[1] Patent: WO2013/140148, 2013, A1. Location in patent: Page/Page column 65
[2] Journal of Medicinal Chemistry, 1999, vol. 42, # 14, p. 2706 - 2715
[3] Journal of Medicinal Chemistry, 1999, vol. 42, # 24, p. 4981 - 5001
[4] Bioorganic and Medicinal Chemistry, 2003, vol. 11, # 24, p. 5345 - 5352
[5] Patent: WO2007/46550, 2007, A1. Location in patent: Page/Page column 117

1-BENZYL-4-(N-BOC-AMINO) PIPERIDINE 98Supplier

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