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[ CAS No. 28697-07-6 ] {[proInfo.proName]}

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Chemical Structure| 28697-07-6
Chemical Structure| 28697-07-6
Structure of 28697-07-6 * Storage: {[proInfo.prStorage]}

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Product Details of [ 28697-07-6 ]

CAS No. :28697-07-6 MDL No. :MFCD01863568
Formula : C14H17NO4 Boiling Point : -
Linear Structure Formula :- InChI Key :ZSAIHAKADPJIGN-UHFFFAOYSA-N
M.W : 263.29 Pubchem ID :4431026
Synonyms :
Chemical Name :N-Cbz-2-Piperidinecarboxylic acid

Calculated chemistry of [ 28697-07-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 19
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.43
Num. rotatable bonds : 5
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 73.2
TPSA : 66.84 ?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) : -6.42 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.29
Log Po/w (XLOGP3) : 2.1
Log Po/w (WLOGP) : 1.73
Log Po/w (MLOGP) : 1.57
Log Po/w (SILICOS-IT) : 1.28
Consensus Log Po/w : 1.79

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 0.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -2.7
Solubility : 0.526 mg/ml ; 0.002 mol/l
Class : Soluble
Log S (Ali) : -3.13
Solubility : 0.193 mg/ml ; 0.000734 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.36
Solubility : 1.15 mg/ml ; 0.00436 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 2.74

Safety of [ 28697-07-6 ]

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

Application In Synthesis of [ 28697-07-6 ]

* 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.

  • Downstream synthetic route of [ 28697-07-6 ]

[ 28697-07-6 ] Synthesis Path-Downstream   1~4

  • 2
  • [ 28697-07-6 ]
  • [ 74-88-4 ]
  • [ 180609-56-7 ]
YieldReaction ConditionsOperation in experiment
93% With potassium hydrogencarbonate; In N,N-dimethyl-formamide; at 20℃; for 18h; EXAMPLE 36; 2-(2-methylpiperidin-2-yl)-1H-benzimidazole-4-carboxamide; EXAMPLE 36A; 1-benzyl 2-methyl piperidine-1,2-dicarboxylate A solution of 1-[(benzyloxy)carbonyl]piperidine-2-carboxylic acid (5 g) and iodomethane (2.5 mL) in DMF (40 mL) was treated with potassium bicarbonate (3.8 g) and stirred at room temperature for 18 hrs. The reaction mixture was concentrated and the residual oil was partitioned between ethyl acetate and water. The organic phase was concentrated and the residue was purified by flash chromatography (silica gel, ethyl acetate/hexanes) to provide Example 36A (4.88 g, Yield: 93%). MS (DCI/NH3) m/z 278 (M+H)+.
  • 3
  • [ 28697-07-6 ]
  • [ 14252-80-3 ]
  • 4
  • [ 67-56-1 ]
  • [ 28697-07-6 ]
  • [ 180609-56-7 ]
YieldReaction ConditionsOperation in experiment
61% To a solution of 9.41 g (1 eq.) l-(Benzyloxycarbonyl)-2-piperidinecarboxylic acid in 200 mL DCM 0.6 g HOBt (0.11 eq.) and 7.45 g (1.1 eq.) EDC hydrochloride were added and the mixture was stirred vigorously at ambient temperature for 1.5 h. To the solution was added 40 mL methanol. The mixture was stirred overnight, extracted with water, and the organic phase dried over magnesium sulfate. The dry solution was filtered and concentrated in vacuum. The resulting residue was purified by chromatography (ethyl acetate/nTieptane 1 : 1), yielding 6.6 g of the title compound as colorless oil (yield 61%).
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