6-Methyl-3-pyridineethanol

Cat.NO.:A171554 Purity:95%

Product Details of [ 100189-17-1 ]

CAS No. :	100189-17-1
Formula :	C₈H₁₁NO
M.W :	137.18
SMILES Code :	OCCC1=CC=C(C)N=C1
MDL No. :	MFCD09926432
InChI Key :	CRZJKFRQNPDUIV-UHFFFAOYSA-N
Pubchem ID :	13566816

Safety of [ 100189-17-1 ]

GHS Pictogram:
Signal Word:	Warning
Hazard Statements:	H302-H315-H319-H335
Precautionary Statements:	P261-P305+P351+P338

Computational Chemistry of [ 100189-17-1 ] Show Less

Physicochemical Properties

Num. heavy atoms	10
Num. arom. heavy atoms	6
Fraction Csp3	0.38
Num. rotatable bonds	2
Num. H-bond acceptors	2.0
Num. H-bond donors	1.0
Molar Refractivity	40.14
TPSA ? Topological Polar Surface Area: Calculated from Ertl P. et al. 2000 J. Med. Chem.	33.12 Å²

Lipophilicity

Log P_o/w (iLOGP)? iLOGP: in-house physics-based method implemented from Daina A et al. 2014 J. Chem. Inf. Model.	1.66
Log P_o/w (XLOGP3)? XLOGP3: Atomistic and knowledge-based method calculated by XLOGP program, version 3.2.2, courtesy of CCBG, Shanghai Institute of Organic Chemistry	0.83
Log P_o/w (WLOGP)? WLOGP: Atomistic method implemented from Wildman SA and Crippen GM. 1999 J. Chem. Inf. Model.	0.92
Log P_o/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.	0.55
Log P_o/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	1.96
Consensus Log P_o/w? Consensus Log P_o/w: Average of all five predictions	1.18

Water Solubility

Log S (ESOL):? ESOL: Topological method implemented from Delaney JS. 2004 J. Chem. Inf. Model.	-1.53
Solubility	4.09 mg/ml ; 0.0298 mol/l
Class? Solubility class: Log S scale Insoluble < -10 < Poorly < -6 < Moderately < -4 < Soluble < -2 Very < 0 < Highly	Very soluble
Log S (Ali)? Ali: Topological method implemented from Ali J. et al. 2012 J. Chem. Inf. Model.	-1.11
Solubility	10.7 mg/ml ; 0.078 mol/l
Class? Solubility class: Log S scale Insoluble < -10 < Poorly < -6 < Moderately < -4 < Soluble < -2 Very < 0 < Highly	Very 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	-2.62
Solubility	0.332 mg/ml ; 0.00242 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	No
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.	-6.55 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)	1.47

Application In Synthesis of [ 100189-17-1 ]

* 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.

Downstream synthetic route of [ 100189-17-1 ]

[ 100189-17-1 ] Synthesis Path-Downstream 1~11

1
[ 36357-38-7 ]
[ 100189-17-1 ]

References: [1]Journal of the American Chemical Society,1939,vol. 61,p. 2562.

2
[ 140-76-1 ]
[ 104-90-5 ]
[ 56019-64-8 ]
[ 100189-17-1 ]

References: [1]Journal of Organic Chemistry,1986,vol. 51,p. 439 – 445.

3
[ 140-76-1 ]
[ 100189-17-1 ]

References: [1]Organic Letters,2011,vol. 13,p. 2726 – 2729.

4
[ 100189-17-1 ]
Br^(1-)*C₂₁H₂₂N₃⁽¹⁺⁾ [ No CAS ]

References: [1]Organic Letters,2011,vol. 13,p. 2726 – 2729.

5
[ 100189-17-1 ]
[ 1147893-28-4 ]

References: [1]Organic Letters,2011,vol. 13,p. 2726 – 2729.

6
[ 100189-17-1 ]
[ 3613-73-8 ]

References: [1]Organic Letters,2011,vol. 13,p. 2726 – 2729.

7
diethyl 2-(6-methylpyridin-3-yl)malonate [ No CAS ]
[ 100189-17-1 ]

References: [1]Patent: WO2014/198808,2014,A1 .
[2]Patent: EP2813505,2014,A1 .

8
[ 3430-13-5 ]
[ 100189-17-1 ]

References: [1]Patent: WO2014/198808,2014,A1 .
[2]Patent: EP2813505,2014,A1 .

9
[ 19733-96-1 ]
[ 100189-17-1 ]

Yield	Reaction Conditions	Operation in experiment
	With dimethylsulfide borane complex; In tetrahydrofuran; at 0 – 20℃; for 1.0h;	To a stirred solution of 2-(6-methylpyridin-3-yl) acetic acid (1 .5g, 9.9 mmol) in dry THF(20 mL) was added Borane-DMS (2 mL, 19.8 mmol) drop wise at 0 00. The reactionmixture was stirred at RT for lh. Reaction completion was monitored by TLC. Reactionmixture was quenched with methanol at 0 00 The reaction mixture was concentratedcompletely and extracted with ethyl acetate, washed with water (2 x 10 mL), sodium bicarbonate (2 x 10 mL) and brine solution (2 x 10 mL). Combined organic layers were dried over anhydrous Na2SO4, filtered, concentrated and the crude mass obtained was purified by flash column chromatography to get the title product as pale yellow liquid. 1HNMR (400 MHz, DMSO-d6): 6 8.55 (s, 1H), 7.93 (dd, J = 8.0, 1.9 Hz, 1H), 7.56 (d, J =8.0 Hz, 1H), 4.74 (s, 1H), 3.65-3.60 (m, 2H), 2.77 (t, J = 6.2 Hz, 2H), 2.59 (s, 3H).LCMS: (Method B) 138.2 (M+H), Rt. 3.5 mm, 91.6% (Max).
	With dimethylsulfide borane complex; In tetrahydrofuran; at 0 – 20℃; for 1.0h;	Step 3: 2-(6-methylpyridin-3-yl) ethan-1-ol To a stirred solution of 2-(6-methylpyridin-3-yl) acetic acid (1.5g, 9.9 mmol) in dry THF (20 mL) was added Borane-DMS (2 mL, 19.8 mmol) drop wise at 0 C. The reaction mixture was stirred at RT for 1 h. Reaction completion was monitored by TLC. Reaction mixture was quenched with methanol at 0 C. The reaction mixture was concentrated completely and extracted with ethyl acetate, washed with water (2 * 10 mL), sodium bicarbonate (2 * 10 mL) and brine solution (2 * 10 mL). Combined organic layers were dried over anhydrous Na2SO4, filtered, concentrated and the crude mass obtained was purified by flash column chromatography to get the title product as pale yellow liquid. 1H NMR (400 MHz, DMSO-d6): delta 8.55 (s, 1 H), 7.93 (dd, J = 8.0, 1.9 Hz, 1 H), 7.56 (d, J = 8.0 Hz, 1 H), 4.74 (s, 1 H), 3.65-3.60 (m, 2H), 2.77 (t, J = 6.2 Hz, 2H), 2.59 (s, 3H). LCMS: (Method B) 138.2 (M+H)+, Rt. 3.5 min, 91.6% (Max).

References: [1]Patent: WO2014/198808,2014,A1 .Location in patent: Page/Page column 141.
[2]Patent: EP2813505,2014,A1 .Location in patent: Paragraph 0222.

10
[ 100189-17-1 ]
(3-chloro-2,4-dimethyl-7H-pyrrolo[3′,4′:3,4]pyrazolo[1,5-a]pyrimidin-8 (9H)-yl)(4-fluoro-2-(2-(6-methylpyridin-3-yl)ethoxy)phenyl)methanone [ No CAS ]

References: [1]Patent: WO2014/198808,2014,A1 .
[2]Patent: EP2813505,2014,A1 .

11
[ 100189-17-1 ]
[ 124-63-0 ]
[ 1189800-65-4 ]

Yield	Reaction Conditions	Operation in experiment
46%	With triethylamine; In dichloromethane; at 0 – 20℃; for 1.0h;	To a stirred solution of <strong>[100189-17-1]2-(6-methylpyridin-3-yl)ethan-1-ol</strong> (0.5 g, 3.6 mmol) in dry DCM(10 mL) at 0 00 was added triethyl amine (1.5 mL, 10.8 mmol, Spectrochem) followed byaddition of methane sulfonyl chloride (0.4 mL, 5.4 mmol, Spectrochem). Reaction mass was brought to RT and stirred for 1 h. Reaction completion was monitored by TLC. Reaction mass was diluted with DCM, washed with water, dried over Na2SO4 and evaporated. The crude was isolated as pale brown liquid and was taken for next stepwithout any further purification (0.36 g, 46%). 1H NMR (400 MHz, DMSO-d6): 6 8.63 (s,1H), 8.00 (dd, J = 8.0, 1.8 Hz, 1H), 7.62-7.58 (m, 1H), 4.45 (t, J = 6.4 Hz, 2H), 3.14 (s,3H), 3.07 (d, J = 6.4 Hz, 2H), 2.59 (s, 3H). LCMS: (Method A) 216.0 (M+H), Rt. 3.3 mm,50.2% (Max).
46%	With triethylamine; In dichloromethane; at 0 – 20℃;	Step 4: 2-(6-methylpyridin-3-yl) ethyl methanesulfonate To a stirred solution of <strong>[100189-17-1]2-(6-methylpyridin-3-yl)ethan-1-ol</strong> (0.5 g, 3.6 mmol) in dry DCM (10 mL) at 0 C was added triethyl amine (1.5 mL, 10.8 mmol, Spectrochem) followed by addition of methane sulfonyl chloride (0.4 mL, 5.4 mmol, Spectrochem). Reaction mass was brought to RT and stirred for 1 h. Reaction completion was monitored by TLC. Reaction mass was diluted with DCM, washed with water, dried over Na2SO4 and evaporated. The crude was isolated as pale brown liquid and was taken for next step without any further purification (0.36 g, 46%). 1H NMR (400 MHz, DMSO-d6): delta 8.63 (s, 1 H), 8.00 (dd, J = 8.0, 1.8 Hz, 1 H), 7.62-7.58 (m, 1 H), 4.45 (t, J = 6.4 Hz, 2H), 3.14 (s, 3H), 3.07 (d, J = 6.4 Hz, 2H), 2.59 (s, 3H). LCMS: (Method A) 216.0 (M+H)+, Rt. 3.3 min, 50.2% (Max).

References: [1]Patent: WO2014/198808,2014,A1 .Location in patent: Page/Page column 141.
[2]Patent: EP2813505,2014,A1 .Location in patent: Paragraph 0223.

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6-Methyl-3-pyridineethanol

Product Details of [ 100189-17-1 ]

Safety of [ 100189-17-1 ]

Computational Chemistry of [ 100189-17-1 ] Show Less

Physicochemical Properties

Lipophilicity

Water Solubility

Pharmacokinetics

Druglikeness

Medicinal Chemistry

Application In Synthesis of [ 100189-17-1 ]

[ 100189-17-1 ] Synthesis Path-Downstream 1~11

Details

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