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[ CAS No. 122860-33-7 ] {[proInfo.proName]}

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Chemical Structure| 122860-33-7
Chemical Structure| 122860-33-7
Structure of 122860-33-7 * Storage: {[proInfo.prStorage]}

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Product Details of [ 122860-33-7 ]

CAS No. :122860-33-7 MDL No. :MFCD02094490
Formula : C14H19NO3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :LINIORCIRVAZSM-UHFFFAOYSA-N
M.W : 249.31 Pubchem ID :736490
Synonyms :

Calculated chemistry of [ 122860-33-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 18
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.5
Num. rotatable bonds : 5
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 72.59
TPSA : 49.77 ?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) : -6.63 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.84
Log Po/w (XLOGP3) : 1.68
Log Po/w (WLOGP) : 1.49
Log Po/w (MLOGP) : 1.68
Log Po/w (SILICOS-IT) : 1.74
Consensus Log Po/w : 1.89

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.36
Solubility : 1.09 mg/ml ; 0.00436 mol/l
Class : Soluble
Log S (Ali) : -2.34
Solubility : 1.14 mg/ml ; 0.00457 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.82
Solubility : 0.377 mg/ml ; 0.00151 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.63

Safety of [ 122860-33-7 ]

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

Application In Synthesis of [ 122860-33-7 ]

* 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.

  • Downstream synthetic route of [ 122860-33-7 ]

[ 122860-33-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 122860-33-7 ]
  • [ 159275-17-9 ]
YieldReaction ConditionsOperation in experiment
10 g With carbon tetrabromide; triphenylphosphine; In dichloromethane; at 20℃; for 3h;Inert atmosphere; To a 500 ml three neck round bottomed flask under nitrogen atmosphere, benzyl 4- (hydroxymethyl) piperidine- l-carboxylate (10 g, 40.1 1 mmol) was dissolved in CH2CI2 (100 ml) and cooled to 0 C. Triphenyl phosphine (13.7 g, 52.14 mmol) in CH2CI2 (50 ml) was added to the reaction mixture and stirred at 0 C for 20 minutes. Carbon tetra bromide (16 g, 48.13 mmol) in CH2CI2 (50 ml) was added to reaction mixture which was stirred at rt for 3 h. The reaction mixture was diluted with CH2CI2 and washed with water. Organic layer was dried over sodium sulfate and concentrated under vacuum and purified by column chromatography to give 10 g of benzyl 4-(bromomethyl) piperidine- l-carboxylate.
  • 2
  • [ 558-13-4 ]
  • [ 122860-33-7 ]
  • [ 159275-17-9 ]
YieldReaction ConditionsOperation in experiment
With triphenylphosphine; In dichloromethane; Step 3 4-Bromomethylpiperidine-1-carboxylic Acid Benzyl Ester To a solution of 4-hydroxymethylpiperidine-1-carboxylic acid benzyl ester (1.11 g), carbon tetrabromide (1.77 g) in methylene chloride (11 ml) was added triphenylphosphine (1.4 g) with ice-cooling, and the mixture was stirred at room temperature for 5 hours. After completion of the reaction, the solvent was evaporated and the obtained residue was purified by silica gel column chromatography (hexane:acetone=10:1) and dried under reduced pressure to give the title compound (1.25 g). 1H-NMR (delta ppm, CDCl3) 1.05-1.30 (m, 2H), 1.70-1.90 (m, 3H), 2.78 (m, 2H), 3.29 (d, 2H), 4.10-4.30 (m, 2H), 5.13 (s, 2H), 7.26-7.38 (m, 5H).
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