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[ CAS No. 142851-03-4 ] {[proInfo.proName]}

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Chemical Structure| 142851-03-4
Chemical Structure| 142851-03-4
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Product Details of [ 142851-03-4 ]

CAS No. :142851-03-4 MDL No. :MFCD01763998
Formula : C13H23NO4 Boiling Point : No data available
Linear Structure Formula :- InChI Key :MYHJCTUTPIKNAT-UHFFFAOYSA-N
M.W : 257.33 Pubchem ID :2758812
Synonyms :
Chemical Name :Ethyl N-Boc-piperidine-4-carboxylate

Calculated chemistry of [ 142851-03-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 18
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.85
Num. rotatable bonds : 6
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 72.3
TPSA : 55.84 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.58 cm/s

Lipophilicity

Log Po/w (iLOGP) : 3.27
Log Po/w (XLOGP3) : 1.82
Log Po/w (WLOGP) : 1.82
Log Po/w (MLOGP) : 1.58
Log Po/w (SILICOS-IT) : 1.42
Consensus Log Po/w : 1.98

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 0.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -2.19
Solubility : 1.68 mg/ml ; 0.00652 mol/l
Class : Soluble
Log S (Ali) : -2.61
Solubility : 0.628 mg/ml ; 0.00244 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.76
Solubility : 4.48 mg/ml ; 0.0174 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 2.43

Safety of [ 142851-03-4 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 142851-03-4 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Upstream synthesis route of [ 142851-03-4 ]
  • Downstream synthetic route of [ 142851-03-4 ]

[ 142851-03-4 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 142851-03-4 ]
  • [ 590-17-0 ]
  • [ 495414-81-8 ]
YieldReaction ConditionsOperation in experiment
2.6 g With n-butyllithium; diisopropylamine In tetrahydrofuran; hexane for 12 h; Cooling with ice A)
1-tert-butyl 4-ethyl 4-(cyanomethyl)piperidine-1,4-dicarboxylate
To a mixture of diisopropylamine (4.7 g) and THF (75 mL) was added n-butyllithium hexane solution (1.6 M, 29 mL) under ice-cooling, and the mixture was stirred for 30 min.
To the mixture was added a mixture of 1-tert-butyl 4-ethyl piperidine-1,4-dicarboxylate (6.0 g) and THF (10 mL) under ice-cooling, the mixture was stirred under ice-cooling for 3 hr, and 2-bromoacetonitrile (5.6 g) was added thereto under ice-cooling.
The mixture was stirred for 12 hr, and the solvent was evaporated under reduced pressure.
Water was added thereto, and the mixture was extracted with ethyl acetate.
The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure.
The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (2.6 g).
1H NMR (300 MHz, DMSO-d6) δ 1.21 (3H, t, J = 7.0 Hz), 1.39 (9H, s), 1.43-1.54 (2H, m), 1.90-2.00 (2H, m), 2.87 (2H, s), 2.96-3.12 (2H, m), 3.57-3.67 (2H, m), 4.11-4.22 (2H, m).
Reference: [1] Patent: EP2933247, 2015, A1, . Location in patent: Paragraph 0333
[2] Patent: WO2010/130665, 2010, A1, . Location in patent: Page/Page column 136-137
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