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[ CAS No. 191014-55-8 ] {[proInfo.proName]}

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Chemical Structure| 191014-55-8
Chemical Structure| 191014-55-8
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Product Details of [ 191014-55-8 ]

CAS No. :191014-55-8 MDL No. :MFCD04116335
Formula : C8H6FNO Boiling Point : -
Linear Structure Formula :- InChI Key :HGBKZVIQHCUHRI-UHFFFAOYSA-N
M.W : 151.14 Pubchem ID :2783329
Synonyms :

Calculated chemistry of [ 191014-55-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.12
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 37.61
TPSA : 33.02 ?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) : -5.43 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.9
Log Po/w (XLOGP3) : 2.53
Log Po/w (WLOGP) : 2.13
Log Po/w (MLOGP) : 1.55
Log Po/w (SILICOS-IT) : 2.21
Consensus Log Po/w : 2.06

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.71
Solubility : 0.296 mg/ml ; 0.00196 mol/l
Class : Soluble
Log S (Ali) : -2.87
Solubility : 0.204 mg/ml ; 0.00135 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.87
Solubility : 0.203 mg/ml ; 0.00134 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.6

Safety of [ 191014-55-8 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313 UN#:
Hazard Statements:H302-H312-H319-H332 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 191014-55-8 ]

* 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 [ 191014-55-8 ]
  • Downstream synthetic route of [ 191014-55-8 ]

[ 191014-55-8 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 191014-55-8 ]
  • [ 186590-01-2 ]
YieldReaction ConditionsOperation in experiment
95% With aluminum (III) chloride In toluene at 130℃; for 18 h; A mixture of intermediate 127, 4-fluoro-2-methoxybenzonitrile, (4.53 g, 30 mmol;) and AlCl3 (5.0 g, 37.6 mmol; Aldrich) in anhydrous toluene (30 mL) was stirred at approximately 130 C. for 18 hrs. After cooling, ice water (~50 mL) was added and the resulting mixture extracted with ether (20 mLx2). The combined extracts were washed sequentially with water and brine, then dried (MgSO4), and concentrated in vacuo to provide the title compound (3.90 g, 28.5 mmol, Yield 95percent) as a white solid: 1H NMR (DMSO-d6, 300 MHz) ? ppm: 6.74-6.84 (2H, m, Ar-Hs), 7.71 (1H, dd, J=7 Hz, J=8.5 Hz, Ar-H), 11.64 (1H, s, OH); 13C NMR (DMSO-d6, 75.5 Hz) ? ppm: 95.13 102.45, 102.78, 106.53, 106.83 115.53, 134.68, 134.84, 161.41, 161.58, 163.00, 166.35. HRMS (ESI-) calcd for C7H3NOF (M-H) 136.0199, found 136.0199.
95%
Stage #1: With aluminum (III) chloride In toluene at 130℃; for 18 h;
Stage #2: With water In toluene
A mixture of 4-fluoro-2-methoxybenzonitrile, (4.53 g, 30 mmol;) and AlCl3 (5.0 g, 37.6 mmol; Aldrich) in anhydrous toluene (30 mL) was stirred at approximately 130° C. for 18 hrs. After cooling, ice water (50 mL)was added and the resulting mixture extracted with ether (20 mL.x.2). The combined extracts were washed sequentially with water and brine, then dried (MgSO4), and concentrated in vacuo to provide the title compound (3.90 g, 28.5 mmol, Yield 95percent) as a white solid: 1H NMR (DMSO-d6, 300 MHz) δ ppm: 6.74-6.84 (2H, m, Ar-Hs), 7.71 (1H, dd, J=7 Hz, J=8.5 Hz, Ar-H), 11.64 (1H, s, OH); 13C NMR (DMSO-d6, 75.5 Hz) δ ppm: 95.13 102.45, 102.78, 106.53, 106.83 115.53, 134.68, 134.84,161.41, 161.58, 163.00, 166.35. HRMS (ESI-) calcd for C7H3NOF (M-H) 136.0199, found 136.0199.
95%
Stage #1: With aluminum (III) chloride In toluene at 130℃; for 18 h;
Stage #2: With water In toluene at 0℃;
4-Fluoro-2-hydroxyben.sum.onitrile. A mixture of intermediate 127, 4-fluoro-2- methoxybenzonitrile, (4.53 g, 30 mmol;) and AlCl3 (5.0 g, 37.6 mmol; Aldrich) in anhydrous toluene (30 mL) was stirred at approximately 130 °C for 18 hrs. After cooling, ice water (~50 mL)was added and the resulting mixture extracted with ether (20 mL x 2). The combined extracts were washed sequentially with water and brine, then dried (MgSO4), and concentrated in vacuo to provide the title compound (3.90 g, 28.5 mmol, Yield 95percent) as a white solid: 1H NMR (DMSO-d6, 300 MHz) δ ppm: 6.74-6.84 (2H, m, Ar-Hs), 7.71 (IH, dd, J = 7 Hz, J = 8.5 Hz, Ar-H), 11.64 (IH, s, OH); 13C NMR (DMSO-d6, 75.5 Hz) δ ppm: 95.13 102.45, 102.78, 106.53, 106.83 115.53, 134.68, 134.84, 161.41, 161.58, 163.00, 166.35.HRMS (ESI-) calcd for C7H3NOF (M-H) 136.0199, found 136.0199.
Reference: [1] Patent: US2005/267105, 2005, A1, . Location in patent: Page/Page column 67
[2] Patent: US2007/111984, 2007, A1, . Location in patent: Page/Page column 33
[3] Patent: WO2007/64316, 2007, A1, . Location in patent: Page/Page column 153
[4] Patent: WO2007/39172, 2007, A1, . Location in patent: Page/Page column 157-158
[5] Patent: US2008/261979, 2008, A1, . Location in patent: Page/Page column 74
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