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Chemical Structure| 52927-22-7

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Product Details of [ 52927-22-7 ]

CAS No. :52927-22-7
Formula : C11H7NO
M.W : 169.18
SMILES Code : C(#N)C2=CC=C1C=C(C=CC1=C2)O
MDL No. :MFCD01863480
InChI Key :WKTNIBWKHNIPQR-UHFFFAOYSA-N
Pubchem ID :4589476

Safety of [ 52927-22-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Computational Chemistry of [ 52927-22-7 ] Show Less

Physicochemical Properties

Num. heavy atoms 13
Num. arom. heavy atoms 10
Fraction Csp3 0.0
Num. rotatable bonds 0
Num. H-bond acceptors 2.0
Num. H-bond donors 1.0
Molar Refractivity 50.69
TPSA ?

Topological Polar Surface Area: Calculated from
Ertl P. et al. 2000 J. Med. Chem.

44.02 Ų

Lipophilicity

Log Po/w (iLOGP)?

iLOGP: in-house physics-based method implemented from
Daina A et al. 2014 J. Chem. Inf. Model.

1.64
Log Po/w (XLOGP3)?

XLOGP3: Atomistic and knowledge-based method calculated by
XLOGP program, version 3.2.2, courtesy of CCBG, Shanghai Institute of Organic Chemistry

1.97
Log Po/w (WLOGP)?

WLOGP: Atomistic method implemented from
Wildman SA and Crippen GM. 1999 J. Chem. Inf. Model.

2.42
Log Po/w (MLOGP)?

MLOGP: Topological method implemented from
Moriguchi I. et al. 1992 Chem. Pharm. Bull.
Moriguchi I. et al. 1994 Chem. Pharm. Bull.
Lipinski PA. et al. 2001 Adv. Drug. Deliv. Rev.

1.82
Log Po/w (SILICOS-IT)?

SILICOS-IT: Hybrid fragmental/topological method calculated by
FILTER-IT program, version 1.0.2, courtesy of SILICOS-IT, http://www.silicos-it.com

2.46
Consensus Log Po/w?

Consensus Log Po/w: Average of all five predictions

2.06

Water Solubility

Log S (ESOL):?

ESOL: Topological method implemented from
Delaney JS. 2004 J. Chem. Inf. Model.

-2.7
Solubility 0.338 mg/ml ; 0.002 mol/l
Class?

Solubility class: Log S scale
Insoluble < -10 < Poorly < -6 < Moderately < -4 < Soluble < -2 Very < 0 < Highly

Soluble
Log S (Ali)?

Ali: Topological method implemented from
Ali J. et al. 2012 J. Chem. Inf. Model.

-2.52
Solubility 0.511 mg/ml ; 0.00302 mol/l
Class?

Solubility class: Log S scale
Insoluble < -10 < Poorly < -6 < Moderately < -4 < Soluble < -2 Very < 0 < Highly

Soluble
Log S (SILICOS-IT)?

SILICOS-IT: Fragmental method calculated by
FILTER-IT program, version 1.0.2, courtesy of SILICOS-IT, http://www.silicos-it.com

-3.58
Solubility 0.0448 mg/ml ; 0.000265 mol/l
Class?

Solubility class: Log S scale
Insoluble < -10 < Poorly < -6 < Moderately < -4 < Soluble < -2 Very < 0 < Highly

Soluble

Pharmacokinetics

GI absorption?

Gatrointestinal absorption: according to the white of the BOILED-Egg

High
BBB permeant?

BBB permeation: according to the yolk of the BOILED-Egg

Yes
P-gp substrate?

P-glycoprotein substrate: SVM model built on 1033 molecules (training set)
and tested on 415 molecules (test set)
10-fold CV: ACC=0.72 / AUC=0.77
External: ACC=0.88 / AUC=0.94

No
CYP1A2 inhibitor?

Cytochrome P450 1A2 inhibitor: SVM model built on 9145 molecules (training set)
and tested on 3000 molecules (test set)
10-fold CV: ACC=0.83 / AUC=0.90
External: ACC=0.84 / AUC=0.91

Yes
CYP2C19 inhibitor?

Cytochrome P450 2C19 inhibitor: SVM model built on 9272 molecules (training set)
and tested on 3000 molecules (test set)
10-fold CV: ACC=0.80 / AUC=0.86
External: ACC=0.80 / AUC=0.87

No
CYP2C9 inhibitor?

Cytochrome P450 2C9 inhibitor: SVM model built on 5940 molecules (training set)
and tested on 2075 molecules (test set)
10-fold CV: ACC=0.78 / AUC=0.85
External: ACC=0.71 / AUC=0.81

No
CYP2D6 inhibitor?

Cytochrome P450 2D6 inhibitor: SVM model built on 3664 molecules (training set)
and tested on 1068 molecules (test set)
10-fold CV: ACC=0.79 / AUC=0.85
External: ACC=0.81 / AUC=0.87

No
CYP3A4 inhibitor?

Cytochrome P450 3A4 inhibitor: SVM model built on 7518 molecules (training set)
and tested on 2579 molecules (test set)
10-fold CV: ACC=0.77 / AUC=0.85
External: ACC=0.78 / AUC=0.86

No
Log Kp (skin permeation)?

Skin permeation: QSPR model implemented from
Potts RO and Guy RH. 1992 Pharm. Res.

-5.93 cm/s

Druglikeness

Lipinski?

Lipinski (Pfizer) filter: implemented from
Lipinski CA. et al. 2001 Adv. Drug Deliv. Rev.
MW ≤ 500
MLOGP ≤ 4.15
N or O ≤ 10
NH or OH ≤ 5

0.0
Ghose?

Ghose filter: implemented from
Ghose AK. et al. 1999 J. Comb. Chem.
160 ≤ MW ≤ 480
-0.4 ≤ WLOGP ≤ 5.6
40 ≤ MR ≤ 130
20 ≤ atoms ≤ 70

None
Veber?

Veber (GSK) filter: implemented from
Veber DF. et al. 2002 J. Med. Chem.
Rotatable bonds ≤ 10
TPSA ≤ 140

0.0
Egan?

Egan (Pharmacia) filter: implemented from
Egan WJ. et al. 2000 J. Med. Chem.
WLOGP ≤ 5.88
TPSA ≤ 131.6

0.0
Muegge?

Muegge (Bayer) filter: implemented from
Muegge I. et al. 2001 J. Med. Chem.
200 ≤ MW ≤ 600
-2 ≤ XLOGP ≤ 5
TPSA ≤ 150
Num. rings ≤ 7
Num. carbon > 4
Num. heteroatoms > 1
Num. rotatable bonds ≤ 15
H-bond acc. ≤ 10
H-bond don. ≤ 5

1.0
Bioavailability Score?

Abbott Bioavailability Score: Probability of F > 10% in rat
implemented from
Martin YC. 2005 J. Med. Chem.

0.55

Medicinal Chemistry

PAINS?

Pan Assay Interference Structures: implemented from
Baell JB. & Holloway GA. 2010 J. Med. Chem.

0.0 alert
Brenk?

Structural Alert: implemented from
Brenk R. et al. 2008 ChemMedChem

0.0 alert: heavy_metal
Leadlikeness?

Leadlikeness: implemented from
Teague SJ. 1999 Angew. Chem. Int. Ed.
250 ≤ MW ≤ 350
XLOGP ≤ 3.5
Num. rotatable bonds ≤ 7

No; 1 violation:MW<1.0
Synthetic accessibility?

Synthetic accessibility score: from 1 (very easy) to 10 (very difficult)
based on 1024 fragmental contributions (FP2) modulated by size and complexity penaties,
trained on 12'782'590 molecules and tested on 40 external molecules (r2 = 0.94)

1.18

Application In Synthesis of [ 52927-22-7 ]

* 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.

  • Downstream synthetic route of [ 52927-22-7 ]

[ 52927-22-7 ] Synthesis Path-Downstream   1~5

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YieldReaction ConditionsOperation in experiment
93% With triethylamine; In dichloromethane; at 20℃; To a solution of 6-hydroxy-2-naphthonitrile (1.0 g, 5.92 mmol)and Et3N (896 mg, 8.88 mmol) in DCM (1.5 mL) was added Tf2O (2.5 g, 8.88 mmol). After stirring at room temperature overnight, H2O (30 mL) was added and the mixture was extracted with ethyl acetate (30 mL x 3). The combined organic layers were washed with brine (30 mL x 3) and dried over Na2SO4. After concentration and purification by column chromatography (petroleum ether/ethyl acetate = 30:1), 59 was obtained as a white solid (1.65 g, 93%). 1H NMR (400 MHz, CDCl3) d 8.30 (s, 1H), 8.03 (d, J = 9.2 Hz,1H), 7.99 (d, J = 8.4 Hz, 1H), 7.83 (d, J = 1.6 Hz, 1H), 7.73 (d,J = 8.4 Hz, 1H), 7.52 (dd, J = 9.2, 2.4 Hz, 1H).
79.1% With pyridine; In dichloromethane; at 20℃; Step 1: 6-cyanonaphthalen-2-yl trifluoromethanesulfonate [004451 To a mixture of 6-hydroxy-2-naphthonitrile (2.13 g, 12.59 mmol), pyridine (1.29 g, 16.37 mmol) and DCM (30 mL) was added trifluoromethanesulfonic anhydride (3.91 g, 13.85 mmol) via syring in 10 minutes. The reaction mixture was stirred at ft overnight. After the reaction was finished, the reaction mixture was quenched with water (20 mL), and the mixture was poured into DCM (100 mL). The resulting mixture was washed with water (100 mL x 2) and saturated brine (100 mL). The orgaic phase was dried over anhydrous Na2SO4 (15 g), filtered and concentrated in vacuo. The crude was purified by silica column chromatography (PE/EtOAc (v/v) = 4/1) to give the title compound as a white solid (3.00 g, 79.1 %).
78% With triethylamine; In dichloromethane; at 0℃; for 1h; To a stirred solution of 6-hydroxy-2-naphthonitrile N (3.0 g, 17.7 mmol) in DCM (90 mL) were added triethylamine (2.68 g, 26.5 mmol) and triflic anhydride (7.5 g, 26.5 mmol) at 0 C and stirring was continued for an additional 1 h at 0 C. The reaction mixture was partitioned between water and DCM; the organic phase was separated, dried over anhydrous Na2S04, and concentrated under reduced pressure to give crude material. The crude material was purified by column chromatography (Si02, 100-200 mesh) eluting with 3% EtOAc/hexane to afford alcohol O (4.2 g, 13.9 mmol, 78%) as a solid. 1H NMR (200 MHz, CDC13): 58.30 (s, 1 H), 8.00 (app t, 2 H), 7.83 (d, J = 2.6 Hz, 1 H), 7.74 (dd, J = 8.8, 1.8 Hz, 1 H), 7.51 (dd, J = 8.8, 2.2 Hz, 1 H).
78% With triethylamine; In dichloromethane; at 0℃; for 1h; To a stirred solution of 6-hydroxy-2-naphthonitrile N (3.0 g, 17.7 mmol) in DCM (90 mL) were added triethylamine (2.68 g, 26.5 mmol) and triflic anhydride (7.5 g, 26.5 mmol) at 0 C and stirring was continued for an additional 1 h at 0 C. The reaction mixture was partitioned between water and DCM; the organic phase was separated, dried over anhydrous Na2S04, and concentrated under reduced pressure to give crude material. The crude material was purified by column chromatography (Si02, 100-200 mesh) eluting with 3% EtOAc/hexane to afford alcohol O (4.2 g, 13.9 mmol, 78%) as a solid. 1H NMR (200 MHz, CDCb): 5D8.30 (s, 1 H), 8.00 (app t, 2 H), 7.83 (d, 7 = 2.6 Hz, 1 H), 7.74 (dd, 7 = 8.8, 1.8 Hz, 1 H), 7.51 (dd, 7 = 8.8, 2.2 Hz, 1 H).
78% With triethylamine; In dichloromethane; at 0℃; for 1h; To a stirred solution of 6-hydroxy-2-naphthonitrile N (3.0 g, 17.7 mmol) in DCM (90 mL) were added triethylamine (2.68 g, 26.5 mmol) and triflic anhydride (7.5 g, 26.5 mmol) at 0 C and stirring was continued for an additional 1 h at 0 C. The reaction mixture was partitioned between water and DCM; the organic phase was separated, dried over anhydrous Na2S04, and concentrated under reduced pressure to give crude material. The crude material was purified by column chromatography (Si02, 100-200 mesh) eluting with 3% EtOAc/hexane to afford alcohol O (4.2 g, 13.9 mmol, 78%) as a solid. 1H NMR (200 MHz, CDCb): 5D8.30 (s, 1 H), 8.00 (app t, 2 H), 7.83 (d, 7 = 2.6 Hz, 1 H), 7.74 (dd, 7 = 8.8, 1.8 Hz, 1 H), 7.51 (dd, 7 = 8.8, 2.2 Hz, 1 H).
With triethylamine; In ethanol; dichloromethane; EXAMPLE 28B 6-(Trifluoromethanesulfonyloxy)-2-naphthalenecarbonitrile A solution of Example 28A (14.01 g, 82.8 mmol) and triethylamine (9.2 g, 91.1 mmol) in methylene chloride (40 mL) at 0 C. was treated dropwise with trifluoromethylsulfonic anhydride (28 g, 99.4 mmol), warmed to 25 C. for 48 h, concentrated, redissolved in ethanol (50 mL) and triturated with water to precipitate 8.4 g of the title compound. MS (DCI/NH3) m/e 319 (M+NH4)+.
With triethylamine; In dichloromethane; at 0 - 20℃; for 48h; Preparation of 6-cvano-2-naphthalenyl thfluoromethanesulfonateTo a solution of 6-cyano-2-naphthol (1 g, 5.91 mmol) and anhydrous NEt3 (anh.) (1 ml, 7.09 mmol) in CH2CI2 anh. (20 ml) and under an inert atmosphere at 0 0C, triflic anhydride [(CF3SO2)2O, 1.20 ml, 7.09 mmol] was added, dropwise. The reaction was brought to room temperature and was then left to react until there was no starting product observed (48 h). The <n="19"/>reaction mixture was concentrated to dryness and the crude product obtained was suspended in EtOH (5 ml_). Water (5 ml_) was added, the mixture was triturated and the resulting suspension was filtered to give a crude product (1.74 g) as a brownish solid. Purification by column chromatography (SiO2, CH2CI2: cyclohexane, 6/4) yielded the compound of the title (1.56 g, 88%) in the form of a white solid IR (KBr) 3058, 2240, 1809, 1630, 1604, 1425, 1152, 964, 932. 1H NMR (400 MHz, CDCI3) 8.30 (d, J = 0.4 Hz, 1 H), 8.03 (d, J = 8.8 Hz, 1 H), 7.99 (d, J = 8.4 Hz, 1 H), 7.83 (d, J = 2.4 Hz, 1 H), 7.73 (dd, J = 8.8 and 1.4 Hz, 1 H) and 7.52 (dd, J = 8.8 and 2.4 Hz, 1 H).

  • 2
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YieldReaction ConditionsOperation in experiment
75% With pyridine; hydrogenchloride; trifluoromethylsulfonic anhydride; In hexane; ethyl acetate; EXAMPLE 95 Trifluoromethanesulfonic acid 6-cyano -naphthalen-2-yl ester A flame dried flask equipped with a stir bar and rubber septum was charged with dry dichlorornethane (35 mL) and 6-cyano-2-naphthol (3.00 g, 17.73 mmol) fromn Example 94 under an argon atmosphere. To this mixture was added pyridine (7.17 mL, 88.61 mmol), and the resulting solution was chilled to 0 C. Triflic anhydride (3.59 mL, 21.28 mmol) was added slowly by syringe, and the reaction mixture was stirred at 0 C. for 1.5 hours. one half equivalent of triflic anhydride was then added and the reaction mixture was allowed to gradually warm to room temperature over a 16 hour period. The solvents were then removed by rotary evaporation, and the residue was taken up in 200 mL of 1:1 EtOAc and 1N HCl. The organics were washed once more with 1N HCl (100 mL), dried over MgSO4 ,and concentrated. Flash chromatography (hexane to 15% EtOAc/hexane) afforded the desired product as a white solid (3.98 g, 75%). LRMS (electrospray) m/z: 319 (M+18) 1H NMR (CDCl3) δ8.32 (s, 1H), 8.05 (d, 1H, J=9.04 Hz), 8.01 (d, 1H, J=8.54 Hz), 7.85 (d, 1H, J=2.51 Hz), 7.76 (dd, 1H, J=9.04, 1.51 Hz), 7.54 (dd, 1H, J=9.03, 2.51 Hz).
With trifluoromethanesulfonic acid anhydride; triethylamine; In ethanol; dichloromethane; EXAMPLE 13B 6-cyano-2-naphthyl trifluoromethanesulfonate A solution of Example 13A (14.01 g, 82.8 mmol) and triethylamine (9.2 g, 91.1 mmol) in dichloromethane (40 mL) at 0 C. was treated dropwise with trifluoromethanesulfonic anhydride (28 g, 99.4 mmol), warmed to room temperature, stirred for 48 hours, concentrated, dissolved in ethanol, (50 mL) triturated with water, and filtered to provide the desired product. MS (DCI/NH3) m/e 319 (M+NH4)+.
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  • 4
  • [ 1493-13-6 ]
  • [ 52927-22-7 ]
  • [ 145369-29-5 ]
YieldReaction ConditionsOperation in experiment
93% With triethylamine; In dichloromethane; at 20℃; The A42-1 (1.0g, 5.92mmol) was dissolved in dichloromethane (30mL), followed by triethylamine (896mg, 8.88mmol), trifluoromethanesulfonateAnhydride (2.5g, 8.88mmol), stirred at room temperature overnight, quenched with water was added, extracted three times with ethyl acetate, the organic phase was washed with brine, dried over anhydrous sodium sulfateDry, the solvent was distilled off, the residue was purified by column chromatography (petroleum ether: ethyl acetate = 30: 1) to give a white solid (1.65g, 93%).
  • 5
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