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[ CAS No. 642494-37-9 ] {[proInfo.proName]}

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Chemical Structure| 642494-37-9
Chemical Structure| 642494-37-9
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Product Details of [ 642494-37-9 ]

CAS No. :642494-37-9 MDL No. :MFCD08669591
Formula : C14H18BNO2 Boiling Point : No data available
Linear Structure Formula :C8H5NHB(OC(CH3)2)2 InChI Key :QAXZRSICOHKXML-UHFFFAOYSA-N
M.W : 243.11 Pubchem ID :11265016
Synonyms :

Calculated chemistry of [ 642494-37-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 18
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.43
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 74.77
TPSA : 34.25 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : Yes
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : Yes
CYP3A4 inhibitor : Yes
Log Kp (skin permeation) : -5.62 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 3.04
Log Po/w (WLOGP) : 2.47
Log Po/w (MLOGP) : 1.49
Log Po/w (SILICOS-IT) : 2.42
Consensus Log Po/w : 1.88

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.57
Solubility : 0.066 mg/ml ; 0.000271 mol/l
Class : Soluble
Log S (Ali) : -3.43
Solubility : 0.0914 mg/ml ; 0.000376 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.89
Solubility : 0.00314 mg/ml ; 0.0000129 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.92

Safety of [ 642494-37-9 ]

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

Application In Synthesis of [ 642494-37-9 ]

* 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 [ 642494-37-9 ]
  • Downstream synthetic route of [ 642494-37-9 ]

[ 642494-37-9 ] Synthesis Path-Upstream   1~9

  • 1
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YieldReaction ConditionsOperation in experiment
25 g With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium acetate In dimethyl sulfoxide at 85℃; for 2 h; 7-bromoindole (20 g, 0.102mol) was dissolved in DMSO (100mL) in an 1 L single neck flask, and bis(pinacolato)diboron (39 g, 0.153 mol), [1,1’-bis(diphenylphosphino)ferrocene]dichloropalladium (Pd(dppf)Cl2, 4 g, 0.005 mol),and potassium acetate (15 g, 0.153 mol) were added. The system was heated to 85 °C to react for 2 h. Water was addedto quench the reaction. The mixture was extracted with ethyl acetate for 3 times, dried over sodium sulfate, concentrated,and subjected to column chromatography to obtain the product (25 g, 0.103 mol). 1H NMR (400 MHz, CDCl3): δ 9.29(s, 1H), 7.82 (d, J = 7.9 Hz, 1H), 7.70 (d, J = 7.0 Hz, 1H), 7.32-7.29 (m, 1H), 7.21-7.14 (m, 1H), 6.62-6.57 (m, 1H), 1.44(s, 12H). MS (ESI) (m/z): [M+H]+ 244.1.
Reference: [1] Synlett, 2003, # 8, p. 1204 - 1206
[2] Advanced Synthesis and Catalysis, 2017, vol. 359, # 19, p. 3421 - 3427
[3] Journal of the American Chemical Society, 2017, vol. 139, # 24, p. 8267 - 8276
[4] European Journal of Organic Chemistry, 2016, vol. 2016, # 27, p. 4621 - 4628
[5] Patent: JP2015/528445, 2015, A, . Location in patent: Paragraph 0047; 0065
[6] Patent: EP3345906, 2018, A1, . Location in patent: Paragraph 0332; 0333
  • 2
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Reference: [1] Journal of Organic Chemistry, 2006, vol. 71, # 15, p. 5807 - 5810
[2] Patent: WO2006/10142, 2006, A2, . Location in patent: Page/Page column 83; 84
  • 3
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Reference: [1] European Journal of Organic Chemistry, 2017, vol. 2017, # 27, p. 4044 - 4053
  • 4
  • [ 116491-57-7 ]
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Reference: [1] Journal of the American Chemical Society, 2006, vol. 128, # 49, p. 15552 - 15553
  • 5
  • [ 25015-63-8 ]
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Reference: [1] Journal of the American Chemical Society, 2006, vol. 128, # 49, p. 15552 - 15553
  • 6
  • [ 51417-51-7 ]
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Reference: [1] Heterocycles, 2010, vol. 80, # 2, p. 1267 - 1274
[2] Patent: US2015/318483, 2015, A1,
  • 7
  • [ 73183-34-3 ]
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Reference: [1] Journal of the American Chemical Society, 2010, vol. 132, # 12, p. 4068 - 4069
  • 8
  • [ 73183-34-3 ]
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Reference: [1] Organic Letters, 2016, vol. 18, # 7, p. 1554 - 1557
  • 9
  • [ 120-72-9 ]
  • [ 642494-37-9 ]
Reference: [1] Organic Letters, 2016, vol. 18, # 7, p. 1554 - 1557
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