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[ CAS No. 225366-90-5 ] {[proInfo.proName]}

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3d Animation Molecule Structure of 225366-90-5
Chemical Structure| 225366-90-5
Chemical Structure| 225366-90-5
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Product Details of [ 225366-90-5 ]

CAS No. :225366-90-5 MDL No. :MFCD22690583
Formula : C9H5BrFN Boiling Point : -
Linear Structure Formula :- InChI Key :LXCKAJPCLUODAF-UHFFFAOYSA-N
M.W : 226.05 Pubchem ID :71239308
Synonyms :

Calculated chemistry of [ 225366-90-5 ]

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 10
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 49.4
TPSA : 12.89 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) : -5.46 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.21
Log Po/w (XLOGP3) : 3.13
Log Po/w (WLOGP) : 3.56
Log Po/w (MLOGP) : 2.98
Log Po/w (SILICOS-IT) : 3.54
Consensus Log Po/w : 3.08

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.83
Solubility : 0.0334 mg/ml ; 0.000148 mol/l
Class : Soluble
Log S (Ali) : -3.07
Solubility : 0.192 mg/ml ; 0.000851 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.84
Solubility : 0.00327 mg/ml ; 0.0000145 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.7

Safety of [ 225366-90-5 ]

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 [ 225366-90-5 ]

* 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 [ 225366-90-5 ]

[ 225366-90-5 ] Synthesis Path-Downstream   1~9

  • 2
  • [ 396-32-7 ]
  • [ 506-68-3 ]
  • [ 79-15-2 ]
  • [ 225366-90-5 ]
  • 3
  • [ 225366-90-5 ]
  • 3,7-Difluoroquinoline [ No CAS ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: c-NH3 aq.; CuSO4*5H2O / 20 h / 160 °C 2: 67 percent / Et4NF; NaNO2 / 1.5 h / 0 - 95 °C
  • 4
  • [ 399-51-9 ]
  • [ 75-25-2 ]
  • [ 225366-90-5 ]
YieldReaction ConditionsOperation in experiment
171.9 mg With N-benzyl-N,N,N-triethylammonium chloride In water; toluene at 40℃; for 16.25h; Intermediate 30: 3-bromo-7-fluoro- 6-Fluoroindole (500 mg, 3.70 mmol) was combined with benzyltriethylammonium chloride (44.4 mg, 0.185 mmol) and toluene (0.32 mL) was added. Bromoform (0.342 mL, 3.70 mmol) was added and the temperature was brought to 40 °C. A solution of NaOH (1 .1 10 g, 7.50 mmol) in water (2.22 mL) was then added over 15 minutes. This caused a very dark color to form. The reaction was stirred as a biphasic mixture at 40 °C for 16 h before cooling and partitioning between ethyl acetate and water. The separated aqueous layer was extracted with ethyl acetate and the combined organics dried over MgS04. Purification by silica gel flash chromatography (ethyl acetate / heptane) gave 3-bromo-7-fluoro-quinoline (171 .9 mg) as a white solid. 1 H NMR (400 MHz, CDCI3) δ 8.93 (d, J=2A Hz, 1 H) 8.33 (d, J=2.0 Hz, 1 H) 7.68 - 7.82 (m, 2 H) 7.39 (td, J=8.6, 2.5 Hz, 1 H); MS (M+1 ): 226.0.
  • 5
  • [ 823-96-1 ]
  • [ 225366-90-5 ]
  • [ 1286756-89-5 ]
YieldReaction ConditionsOperation in experiment
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate In 1,4-dioxane at 90℃; for 15h; Inert atmosphere; Intermediate 31 : 7-fluoro-3-methyl-quinoline 3-bromo-7-fluoro-quinoline (Intermediate 30) (100 mg, 0.442 mmol) was combined with K2CO3 (153 mg, 1 .10 mmol), anhydrous 1 ,4-dioxane (3 ml_), and trimethylboroxine (0.092 ml_, 0.663 mmol). Nitrogen was bubbled in to degas the reaction and Pd(PPh3)4 (50.9 mg, 0.044 mmol) was added. This was degassed again and then heated to 90 °C for 5 h. The reaction was cooled and partitioned between ethyl acetate and sat. aq. NaHC03. The separated aqueous layer was extracted with ethyl acetate and the combined organics dried over MgS04. Purification by silica gel flash chromatography (ethyl acetate / heptane) gave 7-fluoro-3-methyl-quinoline (52.7 mg) as a yellow solid. 1 H NMR (400 MHz, CDCI3) δ 8.78 (d, J=1 .8 Hz, 1 H) 7.93 (s, 1 H) 7.65 - 7.79 (m, 2 H) 7.32 (td, J=8.6, 2.5 Hz, 1 H) 2.52 (s, 3 H); MS (M+1 ): 162.1 .
  • 6
  • [ 225366-90-5 ]
  • [ 1421348-49-3 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 4 steps 1: chloro(2-dicyclohexylphosphino-3,6-dimethoxy-2',4',6'-triisopropyl-1,1'-biphenyl)[2-(2-aminoethyl)phenyl]palladium(ll); lithium hexamethyldisilazane / tetrahydrofuran / 18 h / 65 °C 2: trifluoroacetic acid / dichloromethane / 1.5 h / 20 °C 3: triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; 1-hydroxy-7-aza-benzotriazole / dichloromethane / 2 h 4: sodium hydroxide / tetrahydrofuran; methanol / 18 h / 20 °C
  • 7
  • [ 225366-90-5 ]
  • [ 1421348-81-3 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: chloro(2-dicyclohexylphosphino-3,6-dimethoxy-2',4',6'-triisopropyl-1,1'-biphenyl)[2-(2-aminoethyl)phenyl]palladium(ll); lithium hexamethyldisilazane / tetrahydrofuran / 18 h / 65 °C 2: trifluoroacetic acid / dichloromethane / 1.5 h / 20 °C
  • 8
  • [ 225366-90-5 ]
  • [ 1421348-82-4 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: chloro(2-dicyclohexylphosphino-3,6-dimethoxy-2',4',6'-triisopropyl-1,1'-biphenyl)[2-(2-aminoethyl)phenyl]palladium(ll); lithium hexamethyldisilazane / tetrahydrofuran / 18 h / 65 °C 2: trifluoroacetic acid / dichloromethane / 1.5 h / 20 °C 3: triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; 1-hydroxy-7-aza-benzotriazole / dichloromethane / 2 h
  • 9
  • [ 1421348-79-9 ]
  • [ 225366-90-5 ]
  • [ 1421348-80-2 ]
YieldReaction ConditionsOperation in experiment
10% With chloro(2-dicyclohexylphosphino-3,6-dimethoxy-2',4',6'-triisopropyl-1,1'-biphenyl)[2-(2-aminoethyl)phenyl]palladium(ll); lithium hexamethyldisilazane In tetrahydrofuran at 65℃; for 18h; Intermediate 37: tert-butyl 4-((3,3-dimethylcyclobutyl)(7-fluoroquinolin-3- ylamino)methyl)benzoate To a solution containing chloro(2-dicyclohexylphosphino-3,6-dimethoxy-2',4',6'- triisopropyl-1 , 1 '-biphenyl)[2-(2-aminoethyl)phenyl]palladium(ll) (1 1 .2 mg, 0.0140 mmol) and (Intermediate 30) 3-bromo-7-fluoroquinoline (65.6 mg, 0.290 mmol) was added anhydrous tetrahydrofuran (1 .00 ml.) and a solution of terf-butyl 4-(amino(3,3- dimethylcyclobutyl)methyl)benzoate (80.0 mg, 0.280 mmol) in anhydrous tetrahydrofuran (0.380 ml_). Lithium hexamethyldisilazide (0.690 ml_, 0.690 mmol, 1 M in THF) was added dropwise. The clear, slightly yellow solution became green, yellow, then brown. The reaction was heated at 65 °C for 18 h. The reaction was then cooled to room temperature and diluted with water and extracted three times with ethyl acetate. The combined organic layers were dried with sodium sulfate, filtered, and concentrated to give 138 mg of a brown oil. Purification by silica gel flash chromatography (0-30% ethyl acetate in heptane) afforded tert-butyl 4-((3,3-dimethylcyclobutyl)(7-fluoroquinolin- 3-ylamino)methyl) benzoate (12.0 mg, 10% yield) as a brown oil. 1 H NMR (400 MHz, CDCI3, δ): 8.55 - 8.48 (m, 1 H), 7.97 - 7.90 (m, 2H), 7.59 - 7.52 (m, 1 H), 7.42 (d, J = 8.4 Hz, 2H), 7.40 - 7.33 (m, 1 H), 7.14 (td, J = 8.7, 2.7 Hz, 1 H), 6.71 (d, J = 2.7 Hz, 1 H), 4.24 (dd, J = 9.1 , 4.2 Hz, 1 H), 2.53 (q, J = 8.8 Hz, 1 H), 2.08 - 1 .98 (m, 1 H), 1 .72 (t, J = 9.7 Hz, 2H), 1 .67 - 1.59 (m, 1 H), 1 .57 (s, 9H), 1 .13 (s, 3H), 1.09 (s, 3H). MS (M+1 ): 435.3.
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