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[ CAS No. 915226-44-7 ] {[proInfo.proName]}

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Chemical Structure| 915226-44-7
Chemical Structure| 915226-44-7
Structure of 915226-44-7 * Storage: {[proInfo.prStorage]}

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Product Details of [ 915226-44-7 ]

CAS No. :915226-44-7 MDL No. :MFCD05864632
Formula : C11H18N2O2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :UEFZTXGFHKPSFS-VIFPVBQESA-N
M.W : 210.27 Pubchem ID :7019448
Synonyms :

Calculated chemistry of [ 915226-44-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.82
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 61.15
TPSA : 53.33 ?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) : -6.65 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.5
Log Po/w (XLOGP3) : 1.32
Log Po/w (WLOGP) : 1.78
Log Po/w (MLOGP) : 1.05
Log Po/w (SILICOS-IT) : 1.06
Consensus Log Po/w : 1.54

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.78
Solubility : 3.51 mg/ml ; 0.0167 mol/l
Class : Very soluble
Log S (Ali) : -2.04
Solubility : 1.91 mg/ml ; 0.0091 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.37
Solubility : 9.05 mg/ml ; 0.0431 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.74

Safety of [ 915226-44-7 ]

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 [ 915226-44-7 ]

* 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 [ 915226-44-7 ]
  • Downstream synthetic route of [ 915226-44-7 ]

[ 915226-44-7 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 915226-43-6 ]
  • [ 915226-44-7 ]
YieldReaction ConditionsOperation in experiment
100% at 0 - 20℃; 2(B)
(R)-3-Cyano-piperidine-1-carboxylic acid tert-butyl ester
Phosphorus oxychloride (203 μL, 2.18 mmol) was added dropwise at 0° C. to a solution of (R)-3-carbamoyl-piperidine-1-carboxylic acid tert-butyl ester (0.5 g, 2.18 mmol) in pyridine (10 mL), under nitrogen atmosphere.
After stirring overnight at room temperature, ethyl acetate was added and the solution was washed with 10percent HCl (2 times).
The phases were separated and the organics were dried over sodium sulphate and evaporated to dryness under reduced pressure.
The title compound was used for the next step without further purification.
Yield: quantitative; LCMS (T): 4.48 min (Method A); MS (ES+) gave m/z: 211.1.
Reference: [1] Patent: US2009/215822, 2009, A1, . Location in patent: Page/Page column 10
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