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[ CAS No. 705262-55-1 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 705262-55-1
Chemical Structure| 705262-55-1
Structure of 705262-55-1 * Storage: {[proInfo.prStorage]}
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Quality Control of [ 705262-55-1 ]

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Product Details of [ 705262-55-1 ]

CAS No. :705262-55-1 MDL No. :MFCD09864901
Formula : C7H6BrN3 Boiling Point : -
Linear Structure Formula :- InChI Key :PGSBYVUIXGOCGV-UHFFFAOYSA-N
M.W : 212.05 Pubchem ID :28875375
Synonyms :

Calculated chemistry of [ 705262-55-1 ]

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 47.3
TPSA : 43.32 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) : -6.1 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.57
Log Po/w (XLOGP3) : 2.11
Log Po/w (WLOGP) : 1.69
Log Po/w (MLOGP) : 0.87
Log Po/w (SILICOS-IT) : 0.9
Consensus Log Po/w : 1.43

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.09
Solubility : 0.173 mg/ml ; 0.000814 mol/l
Class : Soluble
Log S (Ali) : -2.65
Solubility : 0.474 mg/ml ; 0.00224 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.58
Solubility : 0.551 mg/ml ; 0.0026 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.87

Safety of [ 705262-55-1 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 705262-55-1 ]

* 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 [ 705262-55-1 ]

[ 705262-55-1 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 705262-55-1 ]
  • [ 108-24-7 ]
  • [ 705262-53-9 ]
YieldReaction ConditionsOperation in experiment
83% With pyridine In dichloromethane for 14h; Heating / reflux; 17 Preparation 17; Preparation of N-Acetyl-N-(6-bromo-imidazo[1,2-a]pyridin-3-yl)-acetamide Add trifluoroacetic acid (10 ml) to a solution of (6-bromo-imidazo [1, 2-a] pyridin- 3-YL)- (1, 1, 3, 3-TETRAMETHYL-BUTYL)-AMINE (prepared in a manner similar to Preparation 12; 0.5 g, 1.54 mmol). Reflux for 1 h and concentrate to dryness. Flash chromatography using ethyl ACETATE/METHANOL mixtures gives the off-white solid intermediate 6-bromo- imidazo [1, 2-a] pyridin-3-ylamine ES+m/e 213.6 (bromine isotopes) (M+1). Immediately dissolve intermediate in dichloromethane and add pyridine (1 g, 12.64 mmol) followed by acetic anyhydride (1.5 g, 14.69 mmol) and reflux for 14 h. Concentration followed by purification by flash chromatography gives 0.38 g (83%) of the title compound. ES+ M/E 297.7 (bromine isotopes) (M+1).
  • 2
  • [ 705262-54-0 ]
  • [ 705262-55-1 ]
YieldReaction ConditionsOperation in experiment
100% With hydrogenchloride In isopropyl alcohol at 20℃; for 24h; Inert atmosphere;
With trifluoroacetic acid for 1h; Heating / reflux; 17 Preparation 17; Preparation of N-Acetyl-N-(6-bromo-imidazo[1,2-a]pyridin-3-yl)-acetamide Add trifluoroacetic acid (10 ml) to a solution of (6-bromo-imidazo [1, 2-a] pyridin- 3-YL)- (1, 1, 3, 3-TETRAMETHYL-BUTYL)-AMINE (prepared in a manner similar to Preparation 12; 0.5 g, 1.54 mmol). Reflux for 1 h and concentrate to dryness. Flash chromatography using ethyl ACETATE/METHANOL mixtures gives the off-white solid intermediate 6-bromo- imidazo [1, 2-a] pyridin-3-ylamine ES+m/e 213.6 (bromine isotopes) (M+1). Immediately dissolve intermediate in dichloromethane and add pyridine (1 g, 12.64 mmol) followed by acetic anyhydride (1.5 g, 14.69 mmol) and reflux for 14 h. Concentration followed by purification by flash chromatography gives 0.38 g (83%) of the title compound. ES+ M/E 297.7 (bromine isotopes) (M+1).
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