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[ CAS No. 886365-25-9 ] {[proInfo.proName]}

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Chemical Structure| 886365-25-9
Chemical Structure| 886365-25-9
Structure of 886365-25-9 * Storage: {[proInfo.prStorage]}

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Product Details of [ 886365-25-9 ]

CAS No. :886365-25-9 MDL No. :MFCD07375112
Formula : C8H8BrNO3 Boiling Point : -
Linear Structure Formula :- InChI Key :HSPQMLCPRUPXSD-UHFFFAOYSA-N
M.W : 246.06 Pubchem ID :46311225
Synonyms :

Calculated chemistry of [ 886365-25-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.25
Num. rotatable bonds : 3
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 49.71
TPSA : 48.42 ?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) : -6.59 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.13
Log Po/w (XLOGP3) : 1.7
Log Po/w (WLOGP) : 1.64
Log Po/w (MLOGP) : 1.22
Log Po/w (SILICOS-IT) : 1.89
Consensus Log Po/w : 1.72

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.58
Solubility : 0.647 mg/ml ; 0.00263 mol/l
Class : Soluble
Log S (Ali) : -2.33
Solubility : 1.15 mg/ml ; 0.00465 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.09
Solubility : 0.201 mg/ml ; 0.000818 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.1

Safety of [ 886365-25-9 ]

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 [ 886365-25-9 ]

* 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 [ 886365-25-9 ]

[ 886365-25-9 ] Synthesis Path-Upstream   1~5

  • 1
  • [ 74-88-4 ]
  • [ 886365-25-9 ]
YieldReaction ConditionsOperation in experiment
77% With silver (II) carbonate In toluene at 50℃; for 15 h; To a solution of methyl 5-bromo-2-hydroxy-pyridine-4-carboxylate (20.0 g, 86.2 mmol) in toluene (200 mL) was added silver carbonate (30.9 g, 112.1 mmol) and iodomethane (18.4 g, 129.3 mmol). The reaction mixture was stirred at 50 °C for 15 h and filtered. The filtrate was concentrated under reduced pressure. The residue was purified bycolumn chromatography (silica gel, 100-200 mesh, 0 to 30percent ethyl acetate in petroleum ether) to give methyl 5-bromo-2-methoxy-pyridine-4-carboxylate (16.4g, 77percent) as a white solid, used as is in the next step.
Reference: [1] Patent: WO2018/73193, 2018, A1, . Location in patent: Page/Page column 74
  • 2
  • [ 67-56-1 ]
  • [ 936011-17-5 ]
  • [ 886365-25-9 ]
YieldReaction ConditionsOperation in experiment
14.9 g at 0℃; for 1 h; To a solution of 5-bromo-2-methoxy-pyridine-4-carbaldehyde (23.5 g, 108.8 mmol) in MeOH (100 mL) were successively added a solution of I2 (35.9 mg, 141.4 mmol) in MeOH (75 mL) and a solution of KOH (15.9 g, 282.8 mmol) in MeOH (75 mL) at 0 °C. The resulting mixture was stirred for 1 hr at 0 °C and the reaction was quenched with saturated aqueous NaHS03. The resulting mixture was diluted with DCM (400 mL). The separated organic phase was washed with H20 (150 mL) and brine (150 mL), dried over anhydrous Na2S04 and concentrated in vacuo. The residue was purified by flash column (eluting with PE:EA=20: 1, v:v) to give methyl 5-bromo-2-methoxy-pyridine-4-carboxylate (14.9 g) as a light yellow solid.
Reference: [1] Patent: WO2018/83136, 2018, A1, . Location in patent: Page/Page column 38
  • 3
  • [ 67-56-1 ]
  • [ 886365-22-6 ]
  • [ 886365-25-9 ]
Reference: [1] Patent: US2014/94456, 2014, A1, . Location in patent: Paragraph 0925-026
[2] Patent: WO2015/153683, 2015, A1, . Location in patent: Paragraph 0717
  • 4
  • [ 13472-85-0 ]
  • [ 886365-25-9 ]
Reference: [1] Patent: US2014/94456, 2014, A1,
[2] Patent: WO2015/153683, 2015, A1,
[3] Patent: WO2018/83136, 2018, A1,
  • 5
  • [ 936011-17-5 ]
  • [ 886365-25-9 ]
Reference: [1] Patent: US2014/94456, 2014, A1,
[2] Patent: WO2015/153683, 2015, A1,
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