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[ CAS No. 1124382-72-4 ] {[proInfo.proName]}

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Chemical Structure| 1124382-72-4
Chemical Structure| 1124382-72-4
Structure of 1124382-72-4 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 1124382-72-4 ]

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Product Details of [ 1124382-72-4 ]

CAS No. :1124382-72-4 MDL No. :MFCD16658939
Formula : C6H5BrN4 Boiling Point : No data available
Linear Structure Formula :- InChI Key :SUFKKFLJJMKVJJ-UHFFFAOYSA-N
M.W : 213.04 Pubchem ID :46864069
Synonyms :

Calculated chemistry of [ 1124382-72-4 ]      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 : 45.09
TPSA : 56.21 ?2

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) : -6.83 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.73
Log Po/w (XLOGP3) : 1.09
Log Po/w (WLOGP) : 1.08
Log Po/w (MLOGP) : 1.58
Log Po/w (SILICOS-IT) : 0.45
Consensus Log Po/w : 1.18

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.45
Solubility : 0.751 mg/ml ; 0.00352 mol/l
Class : Soluble
Log S (Ali) : -1.86
Solubility : 2.92 mg/ml ; 0.0137 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.21
Solubility : 1.3 mg/ml ; 0.00612 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.94

Safety of [ 1124382-72-4 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 1124382-72-4 ]

* 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 [ 1124382-72-4 ]

[ 1124382-72-4 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 870774-25-7 ]
  • [ 1124382-72-4 ]
  • 8-(4-(naphthalen-1-yl)phenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-amine [ No CAS ]
YieldReaction ConditionsOperation in experiment
81% With tetrakis(triphenylphosphine) palladium(0); sodium carbonate; In ethanol; water; toluene; at 120℃; for 8h; General procedure: 8-Bromo- [1,2,4] triazolo [1,5-a] pyridin-2-amine 10 g (46.9 mmol) and 9-phenyl-3- (4,4,5,5-tetramethyl-1, 3,2-dioxaborolan-2-yl) to -9H-carbazole 19.1 g (51.6 mmol) was added to 200 mL toluene, 50 mL EtOH, 50 mL H2O. Pd(PPh3)4 2.7 g (2.3 mmol), Na2CO3 14.9 g (141 mmol) was added at 8 hours after 120 was heated to reflux. It was cooled to room temperature and stop the reaction with 300 mL of purified water to the reaction solution. Extract the mixture with E.A 500 mL, and washed with distilled water. The resulting organic layer was dried over anhydrous MgSO4, was evaporated under reduced pressure, and purified by silica gel column chromatography to give the title compound 13.0 g (yield 74%).Reaction with Preparation Example 1 and 4 - (naphthalen-1-yl) phenylboronic acid with the exception of that, the Preparation Example 2 and the same procedure carried out by the desired compound 12.8 g (yield 81%) was obtained.
  • 2
  • [ 1124382-72-4 ]
  • [ 1005206-25-6 ]
  • 8-(4-(trifluoromethylthio)phenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-amine [ No CAS ]
YieldReaction ConditionsOperation in experiment
87% With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; caesium carbonate; In 1,4-dioxane; water; at 100℃; a) 8-(4-(Trifluoromethylthio)phenyl)-ri,2,41triazolori,5-alpyridin-2-amine In a 150 ml round-bottomed flask, 8-bromo-[l,2,4]triazolo[l,5-a]pyridin-2-amine (1.40 g, 6.58 mmol), 4,4,5,5-tetramethyl-2-(4-(trifluoromethylthio)phenyl)-l,3,2-dioxaborolane (2.00 g, 6.58 mmol) and cesium carbonate (4.29 g, 13.2 mmol) were combined with dioxane (80 ml) and water (8.00 ml) to give a white suspension. l,l'-Bis(diphenylphosphino)ferrocene- palladium(II)dichloride dichloromethane complex (481 mg, 658 μπιο) was added. The reaction mixture was heated to 100C and stirred overnight. Chromatography (silica gel, 70 g, ethyl acetate/heptane = 30:70 to 100:0) yielded the title compound as a light brown solid (1.77 g, 87%). MS: m/z = 311.0 [M+H]+.
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