Basic information Safety Supplier Related

tert-butyl 4-(4-aMino-5-isopropoxy-2-Methylphenyl)piperidine-1-carboxylate

Basic information Safety Supplier Related

tert-butyl 4-(4-aMino-5-isopropoxy-2-Methylphenyl)piperidine-1-carboxylate Basic information

Product Name:
tert-butyl 4-(4-aMino-5-isopropoxy-2-Methylphenyl)piperidine-1-carboxylate
Synonyms:
  • tert-butyl 4-(4-aMino-5-isopropoxy-2-Methylphenyl)piperidine-1-carboxylate
  • 4-(4-AMino-5-isopropoxy-2-Methyl-phenyl)-piperidine-1-carboxylic acid tert-butyl ester
  • 1-Piperidinecarboxylic acid, 4-[4-amino-2-methyl-5-(1-methylethoxy)phenyl]-, 1,1-dimethylethyl ester
  • TERT-BUTYL 4-(4-AMINO-5-ISOPROPOXY-2-METHYLPHENYLI,I FE)PIPERIDINE-1-CARBOXYLATE
  • tert-butyl 4-(4-aMino-5-isopropoxy-2-Methylphenyl)piperidine...
  • 4-(1-Boc-4-piperidyl)-2-isopropoxy-5-methylaniline
  • N-Boc-4-(4-amino-5-isopropoxy-2-methylphenyl)piperidine
CAS:
1032903-63-1
MF:
C20H32N2O3
MW:
348.48
Mol File:
1032903-63-1.mol
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tert-butyl 4-(4-aMino-5-isopropoxy-2-Methylphenyl)piperidine-1-carboxylate Chemical Properties

Boiling point:
470.4±45.0 °C(Predicted)
Density 
1.072±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
6.16±0.16(Predicted)
Appearance
White to off-white Solid
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tert-butyl 4-(4-aMino-5-isopropoxy-2-Methylphenyl)piperidine-1-carboxylate Usage And Synthesis

Synthesis

1032903-52-8

1032903-63-1

Tert-butyl 4-(5-isopropyl-2-methyl-4-nitrophenyl)-3,6-dihydropyridine-1-carboxylate (22.6 g, 0.06 mol) was used as a raw material, which was added to methanol (226 mL) with carbon-loaded palladium hydroxide (20% w/w, 2.26 g). The reaction mixture was stirred at 30-40 °C for 5 h in hydrogen pressure (1 MPa). The completion of the reaction was monitored by TLC. Upon completion of the reaction, the catalyst was removed by filtration and the filtrate was concentrated. To the concentrate n-heptane was added and stirred at 0-10 °C for 2 h to crystallize. The crystals were collected by filtration and the filter cake was dried under vacuum at 40-50 °C to afford tert-butyl 4-(4-amino-5-isopropoxy-2-methylphenyl)piperidine-1-carboxylate as a white solid powder (19.9 g, yield: 95.0%).

References

[1] Patent: CN105461616, 2016, A. Location in patent: Paragraph 0031; 0032; 0033
[2] Patent: EP3287463, 2018, A1. Location in patent: Paragraph 0164; 0167
[3] Patent: KR2016/147358, 2016, A. Location in patent: Paragraph 0238-0240
[4] Bioorganic and Medicinal Chemistry Letters, 2015, vol. 25, # 17, p. 3738 - 3743
[5] Patent: CN108276410, 2018, A. Location in patent: Paragraph 0129; 0130; 0131

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