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[ CAS No. 214623-57-1 ] {[proInfo.proName]}

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Chemical Structure| 214623-57-1
Chemical Structure| 214623-57-1
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Quality Control of [ 214623-57-1 ]

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Product Details of [ 214623-57-1 ]

CAS No. :214623-57-1 MDL No. :MFCD00723841
Formula : C8H8N2O Boiling Point : -
Linear Structure Formula :- InChI Key :BZNMIDYUSWEPOM-UHFFFAOYSA-N
M.W : 148.16 Pubchem ID :4102671
Synonyms :

Calculated chemistry of [ 214623-57-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.12
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 42.05
TPSA : 59.04 ?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 : Yes
Log Kp (skin permeation) : -6.54 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.45
Log Po/w (XLOGP3) : 0.94
Log Po/w (WLOGP) : 1.16
Log Po/w (MLOGP) : 0.51
Log Po/w (SILICOS-IT) : 1.07
Consensus Log Po/w : 1.03

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.69
Solubility : 3.04 mg/ml ; 0.0205 mol/l
Class : Very soluble
Log S (Ali) : -1.77
Solubility : 2.54 mg/ml ; 0.0171 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.23
Solubility : 0.868 mg/ml ; 0.00586 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.24

Safety of [ 214623-57-1 ]

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 [ 214623-57-1 ]

* 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 [ 214623-57-1 ]

[ 214623-57-1 ] Synthesis Path-Upstream   1~3

  • 1
  • [ 10496-75-0 ]
  • [ 214623-57-1 ]
YieldReaction ConditionsOperation in experiment
82% With palladium 10% on activated carbon; hydrogen In methanol at 20℃; for 0.5 h; The 2-methoxy-5-nitrobenzyl cyanide (1eq, 220mg, 1.23mmo1), 20mL of methanol, 10mg of palladium on carbon (10percent of mass) were added sequentially in to the 100mL round bottom flask, the bottle connected to the three links, reaction was stirred at room temperature. Vacuum pumping then recharging N2 , repeat this cycle for 3 times , and N2 loading time not less than 5 min. the reaction was allow to react for 30min at room temperature under H2 protection. After the reaction was complete in 30mins , the palladium-carbon was filtered, concentrated, and column chromatography separation (PE: EA = 5: 1) to give 150 mg of product as a white crystalline solid (compound 7). Yield 82percent.
52% With iron; ammonium chloride In ethanol; water for 3 h; Reflux General procedure: 58.2 mol) of the 5-nitro-2-alkoxybenzonitrile prepared in the previous step was added to the reaction flask and the reduced iron powder(223. 8 mmol), ammonium chloride (29. 1 mmol), ethanol (15 mL) and water (45 mL), refluxed for 3 h,Diluted with ethyl acetate (50 mL * 3), washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated to dryness under reduced pressure.The product was purified by column chromatography (ethyl acetate: petroleum ether = 1: 5 to 1: 1) to obtain pure product.
Reference: [1] Patent: CN106892871, 2017, A, . Location in patent: Paragraph 0109; 0112; 0113
[2] Patent: CN105294584, 2016, A, . Location in patent: Paragraph 0018; 0019
[3] Journal of the Chemical Society, 1945, p. 861,864
[4] Chemical Biology and Drug Design, 2018, vol. 91, # 2, p. 526 - 533
  • 2
  • [ 39835-09-1 ]
  • [ 214623-57-1 ]
Reference: [1] Patent: CN105294584, 2016, A,
[2] Chemical Biology and Drug Design, 2018, vol. 91, # 2, p. 526 - 533
  • 3
  • [ 611-20-1 ]
  • [ 214623-57-1 ]
Reference: [1] Patent: CN105294584, 2016, A,
[2] Chemical Biology and Drug Design, 2018, vol. 91, # 2, p. 526 - 533
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