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[ CAS No. 65169-43-9 ] {[proInfo.proName]}

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Chemical Structure| 65169-43-9
Chemical Structure| 65169-43-9
Structure of 65169-43-9 * Storage: {[proInfo.prStorage]}

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Product Details of [ 65169-43-9 ]

CAS No. :65169-43-9 MDL No. :MFCD07375372
Formula : C8H8ClNO2 Boiling Point : -
Linear Structure Formula :- InChI Key :FOKUGIKLNXFRTI-UHFFFAOYSA-N
M.W : 185.61 Pubchem ID :11636946
Synonyms :

Calculated chemistry of [ 65169-43-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.25
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 45.49
TPSA : 39.19 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.99 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.11
Log Po/w (XLOGP3) : 2.03
Log Po/w (WLOGP) : 1.83
Log Po/w (MLOGP) : 1.25
Log Po/w (SILICOS-IT) : 2.29
Consensus Log Po/w : 1.9

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -2.51
Solubility : 0.577 mg/ml ; 0.00311 mol/l
Class : Soluble
Log S (Ali) : -2.48
Solubility : 0.614 mg/ml ; 0.00331 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.1
Solubility : 0.146 mg/ml ; 0.000785 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.82

Safety of [ 65169-43-9 ]

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 [ 65169-43-9 ]

* 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 [ 65169-43-9 ]

[ 65169-43-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 65169-43-9 ]
  • [ 26807-73-8 ]
  • methyl 2-((1-benzyl-1H-indol-5-yl)amino)-5-methylnicotinate [ No CAS ]
YieldReaction ConditionsOperation in experiment
With tris-(dibenzylideneacetone)dipalladium(0); caesium carbonate; 4,5-bis(diphenylphos4,5-bis(diphenylphosphino)-9,9-dimethylxanthenephino)-9,9-dimethylxanthene; In toluene; for 5.5h;Reflux; Inert atmosphere; [Example 124] (1087) (1088) The mixture of 118 mg of <strong>[26807-73-8]1-benzyl-1H-indol-5-amine</strong>, 100 mg of methyl 2-chloro-5-methylnicotinate, 25 mg of tris(dibenzylideneacetone)dipalladium(0), 31 mg of 4,5'-bis(diphenylphosphino)-9,9'-dimethylxanthene, 352 mg of cesium carbonate, and 5 mL of toluene, was heated at reflux for five hours and 30 minutes under a nitrogen atmosphere. The reaction mixture was cooled to room temperature, and ethyl acetate and water were then added thereto. The organic layer was separated, washed with a saturated aqueous sodium chloride solution and dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography (gradient elution with hexane:ethyl acetate = 100:0-70:30). Water and methanol were added to the thus obtained residue, and the solid was collected by filtration to give 60 mg of methyl 2-((1-benzyl-1H-indol-5-yl)amino)-5-methylnicotinate as a yellow solid. 1H-NMR (DMSO-d6) delta: 2.27 (3H, s), 3.88 (3H, s), 5.40 (2H, s), 6.44 (1H, d, J = 2.6 Hz), 7.14-7.39 (7H, m), 7.48 (1H, d, J = 2.6 Hz), 7.95 (1H, d, J = 1.3 Hz), 8.05 (1H, d, J = 2.0 Hz), 8.21 (1H, d, J = 2.0 Hz), 9.82 (1H, s). MS (ESI, m/z): 372 (M+H)+.
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