Alternatived Products of [ 1427377-75-0 ]
Product Details of [ 1427377-75-0 ]
CAS No. : 1427377-75-0
MDL No. : MFCD23705437
Formula :
C7 H4 BrFN2
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 ]
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 ]
1
[ 1427377-75-0 ]
[ 2641029-00-5 ]
Yield Reaction Conditions Operation 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)*CH2 Cl2 ; potassium acetate / 1,4-dioxane / 16 h / 80 °C / Inert atmosphere
2
[ 1427377-75-0 ]
[ 2641029-01-6 ]
Yield Reaction Conditions Operation 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)*CH2 Cl2 ; potassium acetate / 1,4-dioxane / 16 h / 80 °C / Inert atmosphere
3: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2 Cl2 ; potassium acetate / water; 1,4-dioxane / 18 h / 90 °C / Inert atmosphere
3
[ 1427377-75-0 ]
[ 2641029-02-7 ]
Yield Reaction Conditions Operation 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)*CH2 Cl2 ; potassium acetate / 1,4-dioxane / 16 h / 80 °C / Inert atmosphere
3: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2 Cl2 ; 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 ]
Yield Reaction Conditions Operation 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 ]
Yield Reaction Conditions Operation 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)*CH2 Cl2 ; potassium acetate / 1,4-dioxane / 16 h / 80 °C / Inert atmosphere
3: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2 Cl2 ; 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 ]
Yield Reaction Conditions Operation 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)*CH2 Cl2 ; potassium acetate / 1,4-dioxane / 16 h / 80 °C / Inert atmosphere
3: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2 Cl2 ; 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 ]
Yield Reaction Conditions Operation 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)*CH2 Cl2 ; potassium acetate / 1,4-dioxane / 16 h / 80 °C / Inert atmosphere
3: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2 Cl2 ; 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