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[ CAS No. 1427377-75-0 ] {[proInfo.proName]}

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3d Animation Molecule Structure of 1427377-75-0
Chemical Structure| 1427377-75-0
Chemical Structure| 1427377-75-0
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Product Details of [ 1427377-75-0 ]

CAS No. :1427377-75-0 MDL No. :MFCD23705437
Formula : C7H4BrFN2 Boiling Point : -
Linear Structure Formula :- InChI Key :ZFBMAPTXKUFDHS-UHFFFAOYSA-N
M.W : 215.02 Pubchem ID :122715590
Synonyms :

Calculated chemistry of [ 1427377-75-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 43.75
TPSA : 28.68 Ų

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) : -5.95 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.44
Log Po/w (XLOGP3) : 2.34
Log Po/w (WLOGP) : 2.88
Log Po/w (MLOGP) : 2.31
Log Po/w (SILICOS-IT) : 3.13
Consensus Log Po/w : 2.42

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.25
Solubility : 0.12 mg/ml ; 0.000559 mol/l
Class : Soluble
Log S (Ali) : -2.58
Solubility : 0.563 mg/ml ; 0.00262 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.05
Solubility : 0.0192 mg/ml ; 0.0000893 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.77

Safety of [ 1427377-75-0 ]

Signal Word:Warning Class:
Precautionary Statements:P264-P280-P302+P352-P305+P351+P338-P332+P313-P337+P313-P362 UN#:
Hazard Statements:H315-H319 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 1427377-75-0 ]

* 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 [ 1427377-75-0 ]

[ 1427377-75-0 ] Synthesis Path-Downstream   1~7

  • 1
  • [ 1427377-75-0 ]
  • [ 2641029-00-5 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: pyridinium p-toluenesulfonate / dichloromethane; acetonitrile / 48 h 2: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; potassium acetate / 1,4-dioxane / 16 h / 80 °C / Inert atmosphere
  • 2
  • [ 1427377-75-0 ]
  • [ 2641029-01-6 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: pyridinium p-toluenesulfonate / dichloromethane; acetonitrile / 48 h 2: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; potassium acetate / 1,4-dioxane / 16 h / 80 °C / Inert atmosphere 3: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; potassium acetate / water; 1,4-dioxane / 18 h / 90 °C / Inert atmosphere
  • 3
  • [ 1427377-75-0 ]
  • [ 2641029-02-7 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 4 steps 1: pyridinium p-toluenesulfonate / dichloromethane; acetonitrile / 48 h 2: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; potassium acetate / 1,4-dioxane / 16 h / 80 °C / Inert atmosphere 3: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; potassium acetate / water; 1,4-dioxane / 18 h / 90 °C / Inert atmosphere 4: hydrogenchloride / water; dichloromethane / 0.75 h / 20 °C
  • 4
  • [ 110-87-2 ]
  • [ 1427377-75-0 ]
  • [ 2641028-99-9 ]
YieldReaction ConditionsOperation in experiment
With pyridinium p-toluenesulfonate In dichloromethane; acetonitrile for 48h; 107.B Step B: 7-bromo-6-fluoro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole (Int-107b) To a flask containing 7-bromo-6-fluoro-1H-indazole (1.0 g, 4.7 mmol) in dichloromethane (10 mL) was added pyridinium p-toluenesulfonate (117 mg, 0.465 mmol) followed by 3,4-dihydro-2H-pyran (0.85 mL, 9.3 mmol). Acetonitrile (2 mL) was added and the mixture was allowed to stir for 48 hours. After 48 hours, the mixture was concentrated under reduced pressure. The resulting mixture was purified by silica gel column chromatography (0-100% (3:1 ethyl acetate:ethanol) in hexanes) to afford 7-bromo-6-fluoro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole (Int-107b). MS (ESI) m/z 299 [M+H]+.
  • 5
  • [ 1427377-75-0 ]
  • [ CAS Unavailable ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 5 steps 1: pyridinium p-toluenesulfonate / dichloromethane; acetonitrile / 48 h 2: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; potassium acetate / 1,4-dioxane / 16 h / 80 °C / Inert atmosphere 3: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; potassium acetate / water; 1,4-dioxane / 18 h / 90 °C / Inert atmosphere 4: hydrogenchloride / water; dichloromethane / 0.75 h / 20 °C 5: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 3 h / 50 °C
  • 6
  • [ 1427377-75-0 ]
  • [ CAS Unavailable ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 6 steps 1: pyridinium p-toluenesulfonate / dichloromethane; acetonitrile / 48 h 2: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; potassium acetate / 1,4-dioxane / 16 h / 80 °C / Inert atmosphere 3: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; potassium acetate / water; 1,4-dioxane / 18 h / 90 °C / Inert atmosphere 4: hydrogenchloride / water; dichloromethane / 0.75 h / 20 °C 5: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 3 h / 50 °C 6: trifluoroacetic acid / dichloromethane / 1 h / 20 °C
  • 7
  • [ 1427377-75-0 ]
  • [ CAS Unavailable ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 7 steps 1: pyridinium p-toluenesulfonate / dichloromethane; acetonitrile / 48 h 2: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; potassium acetate / 1,4-dioxane / 16 h / 80 °C / Inert atmosphere 3: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; potassium acetate / water; 1,4-dioxane / 18 h / 90 °C / Inert atmosphere 4: hydrogenchloride / water; dichloromethane / 0.75 h / 20 °C 5: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 3 h / 50 °C 6: trifluoroacetic acid / dichloromethane / 1 h / 20 °C 7: N-ethyl-N,N-diisopropylamine / dichloromethane / 0.5 h / 0 °C
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