Basic information Safety Supplier Related

1-Boc-4-Propylaminopiperidine

Basic information Safety Supplier Related

1-Boc-4-Propylaminopiperidine Basic information

Product Name:
1-Boc-4-Propylaminopiperidine
Synonyms:
  • 4-PROPYLAMINO-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
  • 4-PROPYLAMINO-1-BOC-PIPERIDINE
  • 4-Propylamino-1-Boc
  • 1-BOC-4-PROPYLAMINOPIPERIDINE
  • tert-butyl 4-(propylamino)piperidine-1-carboxylate
  • N-Boc-4-propylaminopiperidine
  • 4-(Prop-1-ylamino)piperidine, N1-BOC protected 97%
  • 1-Piperidinecarboxylic acid, 4-(propylamino)-, 1,1-dimethylethyl ester
CAS:
301225-58-1
MF:
C13H26N2O2
MW:
242.36
Mol File:
301225-58-1.mol
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1-Boc-4-Propylaminopiperidine Chemical Properties

Boiling point:
322.6±35.0 °C(Predicted)
Density 
0.99±0.1 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
10.25±0.20(Predicted)
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Safety Information

HS Code 
2933399990
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1-Boc-4-Propylaminopiperidine Usage And Synthesis

Synthesis

107-10-8

79099-07-3

301225-58-1

Step A: N-tert-butoxycarbonyl-4-piperidone (5 g, 25 mmol), n-propylamine (3.69 mL, 45 mmol), acetic acid (1.43 mL, 25 mmol), and sodium triacetoxyborohydride (7.95 g, 37.5 mmol) were dissolved in dichloromethane (100 mL) and the reaction was stirred for 16 h at room temperature. After completion of the reaction, the reaction mixture was washed with deionized water (50 mL) and then with saturated sodium bicarbonate solution. The aqueous phase was back-extracted with dichloromethane (20 mL), and all organic phases were combined, dried with anhydrous magnesium sulfate, and concentrated under reduced pressure to give 1-N-Boc-4-propylaminopiperidine 6 g in 95% yield.

References

[1] Bioorganic and Medicinal Chemistry Letters, 2001, vol. 11, # 18, p. 2475 - 2479
[2] Patent: US6498161, 2002, B1
[3] Bioorganic and Medicinal Chemistry Letters, 2008, vol. 18, # 1, p. 336 - 343

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