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[ CAS No. 167484-91-5 ] {[proInfo.proName]}

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Chemical Structure| 167484-91-5
Chemical Structure| 167484-91-5
Structure of 167484-91-5 * Storage: {[proInfo.prStorage]}

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Product Details of [ 167484-91-5 ]

CAS No. :167484-91-5 MDL No. :MFCD12198573
Formula : C17H23FN2O2 Boiling Point : -
Linear Structure Formula :- InChI Key :MPZQIQHRSUIGMT-UHFFFAOYSA-N
M.W : 306.38 Pubchem ID :49760961
Synonyms :

Calculated chemistry of [ 167484-91-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 22
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.53
Num. rotatable bonds : 3
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 91.34
TPSA : 41.9 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : Yes
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : Yes
CYP2D6 inhibitor : Yes
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.48 cm/s

Lipophilicity

Log Po/w (iLOGP) : 3.22
Log Po/w (XLOGP3) : 2.36
Log Po/w (WLOGP) : 3.47
Log Po/w (MLOGP) : 2.99
Log Po/w (SILICOS-IT) : 3.58
Consensus Log Po/w : 3.12

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.22
Solubility : 0.184 mg/ml ; 0.000606 mol/l
Class : Soluble
Log S (Ali) : -2.88
Solubility : 0.401 mg/ml ; 0.00132 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.36
Solubility : 0.0132 mg/ml ; 0.0000435 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 3.66

Safety of [ 167484-91-5 ]

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

Application In Synthesis of [ 167484-91-5 ]

* 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 [ 167484-91-5 ]

[ 167484-91-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 3012-80-4 ]
  • [ 167484-91-5 ]
  • [ 141-75-3 ]
  • 1-butyryl-5-fluoro-1'-[(1-methyl-1H-benzimidazol-2-yl)methyl]-1,2-dihydrospiro[indole-3,4'-piperidine] [ No CAS ]
YieldReaction ConditionsOperation in experiment
A 2.0 M solution of triethylamine solution in DCE was prepared. 2.0 M stock solutions of amine (XLVII) in this mixture were prepared and sonicated for 10 min. A 0.25 M tetramethylammonium triacetoxyborohydride solution in DCE was prepared and sonicated for 10 min. 0.25 M solutions of aldehyde (III) in DCE were prepared. 1 mL of the solution of amine (XLVII) was dispensed into 2-dram vials. To each vial was added 0.8 mL of the solution of aldehyde (III), and 2.4 mL of the tetramethylammonium triacetoxyborohydride solution. The vials were capped and shaken at room temperature for 16 h. 1.5 mL of 15% NH4OH aqueous solution was added to each vial. The vials were initially slowly then more <n="87"/>vigorously vortexed, centrifuged, and allowed to stand for 2 h. The aqueous layer was discarded and the organic layers were evaporated. 1 mL of DCM and 0.25 mL of TFA was added to each vial. The vials were capped and shaken at room temperature for 16 h. The solvent was evaporated and 1 mL of toluene was added to each vial. The samples were evaporated to dryness. 2 M solution of Et3N and 0.25 M solutions of various acid chlorides in anhydrous DMA were prepared. 1 mL of the Et3N solution was added to each vial and the vials were vortexed until the solutions became clear. 0.96 of the acid chloride solution was added to the corresponding vial and the vials were capped and shaken at room temperature for 16 h. The solvent was evaporated. To each vial was added 3 mL of DCE and 2 mL of water. The vials were vortexed and centrifuged. The orranic layers were transferred into collections vial. The samples were evaporated, dissolved in 1 mL of DMSO, filtered and submitted to HPLC purification.
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