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[ CAS No. 1408282-26-7 ] {[proInfo.proName]}

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Chemical Structure| 1408282-26-7
Chemical Structure| 1408282-26-7
Structure of 1408282-26-7 * Storage: {[proInfo.prStorage]}

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Product Citations

Product Citations

Beckers, Igor ; O'Rourke, Galahad ; De Vos, Dirk DOI:

Abstract: The C-H arylation of indoles holds the promise to shorten synthetic routes in the production of pharmaceuticals. However, late-stage C-H activation reactions often rely on the presence of protecting groups or stoichiometric metal additives. The regiospecific C-H arylation of a highly functionalized azepino[5,3,4-cd]indole scaffold lacking directing groups via Pd(II) and Cu(II) co-catalysis is reported. The direct C-H coupling was demonstrated in the convergent synthesis of rucaparib, an FDA approved anticancer drug.

Keywords: C-H activation ; indole ; arylation ; homogeneous catalysis ; palladium ; copper ; organic synthesis ; pharmaceuticals

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Product Details of [ 1408282-26-7 ]

CAS No. :1408282-26-7 MDL No. :MFCD23381312
Formula : C11H9FN2O Boiling Point : No data available
Linear Structure Formula :- InChI Key :XXKDRTXIEZBWPZ-UHFFFAOYSA-N
M.W : 204.20 Pubchem ID :71503507
Synonyms :

Calculated chemistry of [ 1408282-26-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.18
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 2.0
Molar Refractivity : 58.02
TPSA : 44.89 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : Yes
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.51 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.39
Log Po/w (XLOGP3) : 1.46
Log Po/w (WLOGP) : 1.63
Log Po/w (MLOGP) : 1.68
Log Po/w (SILICOS-IT) : 3.06
Consensus Log Po/w : 1.84

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.47
Solubility : 0.692 mg/ml ; 0.00339 mol/l
Class : Soluble
Log S (Ali) : -2.01
Solubility : 2.0 mg/ml ; 0.0098 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.34
Solubility : 0.00936 mg/ml ; 0.0000458 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.05

Safety of [ 1408282-26-7 ]

Signal Word:Warning Class:
Precautionary Statements:P280 UN#:
Hazard Statements:H302-H317 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 1408282-26-7 ]

* 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 [ 1408282-26-7 ]
  • Downstream synthetic route of [ 1408282-26-7 ]

[ 1408282-26-7 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 1408282-26-7 ]
  • [ 283173-50-2 ]
Reference: [1] Organic Process Research and Development, 2012, vol. 16, # 12, p. 1897 - 1904
[2] Organic Process Research and Development, 2012, vol. 16, # 12, p. 1897 - 1904
[3] ACS Chemical Neuroscience, 2018, vol. 9, # 6, p. 1259 - 1263
[4] Patent: WO2018/140377, 2018, A1,
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