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[ CAS No. 30766-11-1 ] {[proInfo.proName]}

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Chemical Structure| 30766-11-1
Chemical Structure| 30766-11-1
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Product Details of [ 30766-11-1 ]

CAS No. :30766-11-1 MDL No. :MFCD00234149
Formula : C6H4BrNO2 Boiling Point : -
Linear Structure Formula :- InChI Key :MNNQIBXLAHVDDL-UHFFFAOYSA-N
M.W : 202.01 Pubchem ID :608544
Synonyms :

Calculated chemistry of [ 30766-11-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 38.9
TPSA : 50.19 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.54 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.1
Log Po/w (XLOGP3) : 1.4
Log Po/w (WLOGP) : 1.54
Log Po/w (MLOGP) : -0.34
Log Po/w (SILICOS-IT) : 1.43
Consensus Log Po/w : 1.03

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 0.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -2.35
Solubility : 0.897 mg/ml ; 0.00444 mol/l
Class : Soluble
Log S (Ali) : -2.06
Solubility : 1.77 mg/ml ; 0.00875 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.26
Solubility : 1.12 mg/ml ; 0.00555 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.44

Safety of [ 30766-11-1 ]

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

Application In Synthesis of [ 30766-11-1 ]

* 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.

  • Upstream synthesis route of [ 30766-11-1 ]
  • Downstream synthetic route of [ 30766-11-1 ]

[ 30766-11-1 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 30766-11-1 ]
  • [ 1765-93-1 ]
  • [ 845826-99-5 ]
YieldReaction ConditionsOperation in experiment
87.7% With tetrakis(triphenylphosphine) palladium(0); potassium carbonate In 1,2-dimethoxyethane; water at 98℃; for 24 h; Inert atmosphere Step A:5-bromopyridine-2-carboxylic acid (57, 1.0 g, 5.0 mmol)Dissolved in ethylene glycol dimethyl ether (12 mL) and water (4 mL),Add p-fluorophenylboronic acid (17, 1.0 g, 7.5 mmol)And anhydrous potassium carbonate (1.0 g, 7.5 mmol),Then tetrakis(triphenylphosphine)palladium (289 mg, 0.25 mmol) was added.The resulting mixture was stirred at 98 ° C for 24 hours under a nitrogen atmosphere.TLC analysis indicated that the reaction was over,The reaction solution was cooled to room temperature.Then add water (40 mL),The pH was adjusted to 2-3 with 6M hydrochloric acid.Filtered, the filter cake is dissolved in dichloromethane,The organic layer was washed with 20 mL of saturated sodium bicarbonate solution.Divide the water layer,The aqueous layer was adjusted to pH 2-3 with a 6M hydrochloric acid solution.Filter the solid,The filter cake is washed with water to neutrality.The filter cake was dried to give compound 61 (942 mg).Yield: 87.7percent.
Reference: [1] Patent: CN108623532, 2018, A, . Location in patent: Paragraph 0206; 0207; 0208
[2] Patent: EP1657242, 2006, A1, . Location in patent: Page/Page column 31
[3] Bioorganic and Medicinal Chemistry, 2016, vol. 24, # 4, p. 812 - 819
[4] Medicinal Chemistry, 2017, vol. 13, # 2, p. 176 - 185
[5] Medicinal Chemistry Research, 2018, vol. 27, # 2, p. 374 - 387
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