| Identification | Back Directory | [Name]
tert-butyl 4-(4-aMino-5-isopropoxy-2-Methylphenyl)piperidine-1-carboxylate | [CAS]
1032903-63-1 | [Synonyms]
tert-butyl 4-(4-aMino-5-isopropoxy-2-Methylphenyl)piperidine...
tert-butyl 4-(4-aMino-5-isopropoxy-2-Methylphenyl)piperidine-1-carboxylate
TERT-BUTYL 4-(4-AMINO-5-ISOPROPOXY-2-METHYLPHENYLI，I FE)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 | [Molecular Formula]
C20H32N2O3 | [MDL Number]
MFCD26407295 | [MOL File]
1032903-63-1.mol | [Molecular Weight]
348.48 |
| Chemical Properties | Back Directory | [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 |
| Hazard Information | Back Directory | [Synthesis]
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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